A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614965



Internal ID7001854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128097627..128098674hg38UCSC Ensembl
Innerchr7:128097677..128098597hg38UCSC Ensembl
Outerchr7:128097495..128098806hg38UCSC Ensembl
chr7:127737679..127738726hg19UCSC Ensembl
Innerchr7:127737729..127738649hg19UCSC Ensembl
Outerchr7:127737547..127738858hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg381048
hg191048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12962982, essv12962983
SamplesHG03016, HG02728
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614965
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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