A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701800



Internal ID15091766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:79927522..79931130hg38UCSC Ensembl
Innerchr6:80637239..80640847hg19UCSC Ensembl
Innerchr6:80693958..80697566hg18UCSC Ensembl
Innerchr6:80693958..80697566hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg383609
hg193609
hg183609
hg173609
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525646
Supporting Variants
Samples
Known GenesELOVL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701800
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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