A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613890



Internal ID6654098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81712154..81714487hg38UCSC Ensembl
Innerchr7:81712178..81714463hg38UCSC Ensembl
Outerchr7:81712130..81714511hg38UCSC Ensembl
chr7:81341470..81343803hg19UCSC Ensembl
Innerchr7:81341494..81343779hg19UCSC Ensembl
Outerchr7:81341446..81343827hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382334
hg192334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12864873, essv12864872
SamplesNA19652, NA19072
Known GenesHGF
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613890
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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