A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654276



Internal ID15044242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8330828..8349612hg38UCSC Ensembl
Innerchr1:8390888..8409672hg19UCSC Ensembl
Innerchr1:8313475..8332259hg18UCSC Ensembl
Innerchr1:8325154..8343938hg17UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3818785
hg1918785
hg1818785
hg1718785
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516827
Supporting Variants
Samples
Known GenesSLC45A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654276
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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