A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3483488



Internal ID18724443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12469909..12492299hg38UCSC Ensembl
Innerchr10:12511908..12534298hg19UCSC Ensembl
Innerchr10:12551914..12574304hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3822391
hg1922391
hg1822391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036247
Supporting Variants
Samples
Known GenesCAMK1D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3483488
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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