A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614002



Internal ID7000897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85727793..85732041hg38UCSC Ensembl
Innerchr7:85727793..85732041hg38UCSC Ensembl
Outerchr7:85727486..85732270hg38UCSC Ensembl
chr7:85357109..85361357hg19UCSC Ensembl
Innerchr7:85357109..85361357hg19UCSC Ensembl
Outerchr7:85356802..85361586hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg384249
hg194249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12878343
SamplesNA19439
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614002
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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