A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2715626



Internal ID9949913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:9226119..9226764hg38UCSC Ensembl
Outerchr17:9129436..9130081hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38646
hg19646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6898092, essv6725138, essv6867957, essv6688813, essv6913265, essv6932583, essv6682193, essv6713578, essv6901098, essv6780096, essv6776323, essv6753011, essv6835508, essv6800940, essv6741599, essv6792540, essv6924965, essv6706791, essv6816010, essv6936898, essv6928482, essv6759042, essv6831938, essv6750099, essv6895237, essv6843136, essv6858204, essv6732805, essv6738333, essv6871202, essv6796717, essv6784263, essv6717466, essv6674217, essv6953957, essv6905517, essv6828354, essv6920900, essv6971525, essv6901906, essv6912486, essv6803955, essv6960390, essv6728938, essv6806852, essv6949767, essv6966860, essv6685611, essv6747275, essv6885507, essv6839253, essv6877158
SamplesSSM100, SSM071, SSM027, SSM024, SSM045, SSM046, SSM087, SSM013, SSM073, SSM050, SSM074, SSM042, SSM002, SSM057, SSM028, SSM092, SSM084, SSM090, SSM021, SSM047, SSM018, SSM026, SSM089, SSM017, SSM019, SSM035, SSM031, SSM067, SSM001, SSM033, SSM066, SSM068, SSM081, SSM040, SSM072, SSM082, SSM020, SSM015, SSM080, SSM077, SSM010, SSM055, SSM070, SSM095, SSM025, SSM034, SSM099, SSM043, SSM052, SSM098, SSM056, SSM012
Known GenesNTN1
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2715626
Frequency
Sample Size96
Observed Gain0
Observed Loss52
Observed Complex0
Frequencyn/a


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