A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615060



Internal ID7001949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132751287..132761577hg38UCSC Ensembl
Innerchr7:132751287..132761577hg38UCSC Ensembl
Outerchr7:132751103..132761861hg38UCSC Ensembl
chr7:132436047..132446337hg19UCSC Ensembl
Innerchr7:132436047..132446337hg19UCSC Ensembl
Outerchr7:132435863..132446621hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3810291
hg1910291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12973573, essv12973572
SamplesNA21115, NA20867
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615060
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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