A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2745657



Internal ID9979941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:26358095..26358405hg38UCSC Ensembl
Outerchr12:26511028..26511338hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6809377, essv6977177, essv6673146, essv6862374, essv6857192, essv6677812, essv6702449, essv6851174, essv6867152, essv6685078, essv6779458, essv6894639, essv6838622, essv6803508, essv6965768, essv6891278, essv6885084, essv6959258, essv6688287, essv6709491, essv6908874, essv6819684, essv6865621, essv6812215, essv6944951, essv6823619, essv6728328, essv6900645
SamplesSSM100, SSM083, SSM027, SSM075, SSM046, SSM011, SSM079, SSM087, SSM097, SSM039, SSM073, SSM088, SSM041, SSM023, SSM029, SSM026, SSM089, SSM035, SSM032, SSM031, SSM067, SSM014, SSM086, SSM078, SSM076, SSM095, SSM034, SSM098
Known GenesITPR2
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)esv2745657
Frequency
Sample Size96
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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