A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699326



Internal ID15435978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:166382945..166406286hg38UCSC Ensembl
Innerchr6:166796433..166819774hg19UCSC Ensembl
Innerchr6:166716423..166739764hg18UCSC Ensembl
Innerchr6:166766844..166790185hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3823342
hg1923342
hg1823342
hg1723342
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523548
Supporting Variants
Samples
Known GenesMPC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699326
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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