A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674869



Internal ID15064835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12712863..12714150hg38UCSC Ensembl
Innerchr10:12754862..12756149hg19UCSC Ensembl
Innerchr10:12794868..12796155hg18UCSC Ensembl
Innerchr10:12794868..12796155hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381288
hg191288
hg181288
hg171288
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520469
Supporting Variants
Samples
Known GenesCAMK1D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674869
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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