A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2734333



Internal ID10317969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:45432528..45432778hg38UCSC Ensembl
Outerchr7:45472127..45472377hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6963384, essv6935022, essv6731117, essv6808617, essv6723489, essv6930784, essv6889977, essv6715772, essv6690701, essv6797665, essv6919110, essv6952165, essv6845152, essv6865871, essv6671495, essv6975234
SamplesSSM036, SSM075, SSM045, SSM009, SSM021, SSM047, SSM029, SSM089, SSM017, SSM003, SSM031, SSM085, SSM025, SSM004, SSM043, SSM012
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)esv2734333
Frequency
Sample Size96
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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