A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697229



Internal ID15087195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85435157..85538041hg38UCSC Ensembl
Innerchr6:86144875..86247759hg19UCSC Ensembl
Innerchr6:86201594..86304478hg18UCSC Ensembl
Innerchr6:86201594..86304478hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38102885
hg19102885
hg18102885
hg17102885
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520112
Supporting Variants
Samples
Known GenesNT5E, SNX14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697229
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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