A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2715626

Internal ID9949913
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:9226119..9226764hg38UCSC Ensembl
Outerchr17:9129436..9130081hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6725138, essv6674217, essv6920900, essv6928482, essv6717466, essv6688813, essv6901906, essv6713578, essv6803955, essv6885507, essv6738333, essv6936898, essv6971525, essv6877158, essv6828354, essv6932583, essv6924965, essv6816010, essv6706791, essv6835508, essv6895237, essv6960390, essv6966860, essv6732805, essv6728938, essv6831938, essv6858204, essv6949767, essv6776323, essv6839253, essv6901098, essv6685611, essv6780096, essv6898092, essv6843136, essv6800940, essv6953957, essv6747275, essv6792540, essv6912486, essv6750099, essv6759042, essv6871202, essv6784263, essv6682193, essv6867957, essv6913265, essv6753011, essv6796717, essv6806852, essv6741599, essv6905517
SamplesSSM010, SSM027, SSM092, SSM013, SSM082, SSM055, SSM033, SSM084, SSM099, SSM042, SSM040, SSM043, SSM089, SSM090, SSM031, SSM035, SSM025, SSM072, SSM020, SSM071, SSM057, SSM001, SSM024, SSM045, SSM067, SSM050, SSM077, SSM012, SSM100, SSM056, SSM017, SSM066, SSM028, SSM095, SSM047, SSM073, SSM021, SSM002, SSM034, SSM087, SSM046, SSM019, SSM052, SSM068, SSM074, SSM015, SSM026, SSM098, SSM018, SSM081, SSM070, SSM080
Known GenesNTN1
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Pubmed ID23290073
Accession Number(s)esv2715626
Sample Size96
Observed Gain0
Observed Loss52
Observed Complex0

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