A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2733612



Internal ID10317248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:475451..475857hg38UCSC Ensembl
Outerchr7:515088..515494hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6872906, essv6855481, essv6802694, essv6799045, essv6837606, essv6849392, essv6943630, essv6881552, essv6969558, essv6869907, essv6930630, essv6687397, essv6694358, essv6723409, essv6899827, essv6822602, essv6833938, essv6957316, essv6719601, essv6786582, essv6808563, essv6887146, essv6903877
SamplesSSM100, SSM083, SSM075, SSM045, SSM079, SSM087, SSM013, SSM073, SSM023, SSM028, SSM090, SSM069, SSM096, SSM026, SSM035, SSM094, SSM044, SSM086, SSM072, SSM082, SSM020, SSM037, SSM091
Known Genes
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)esv2733612
Frequency
Sample Size96
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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