A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615669



Internal ID7002558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156617809..156627749hg38UCSC Ensembl
Innerchr7:156618309..156627249hg38UCSC Ensembl
Outerchr7:156616809..156628749hg38UCSC Ensembl
chr7:156410503..156420443hg19UCSC Ensembl
Innerchr7:156411003..156419943hg19UCSC Ensembl
Outerchr7:156409503..156421443hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg389941
hg199941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13039700, essv13039701, essv13039702
SamplesHG02792, HG03705, HG03663
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615669
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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