A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695258



Internal ID15085224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12464347..12487196hg38UCSC Ensembl
Innerchr10:12506346..12529195hg19UCSC Ensembl
Innerchr10:12546352..12569201hg18UCSC Ensembl
Innerchr10:12546352..12569201hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3822850
hg1922850
hg1822850
hg1722850
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517854
Supporting Variants
Samples
Known GenesCAMK1D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695258
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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