A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3507137



Internal ID18458732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18185534..18204747hg38UCSC Ensembl
Innerchr10:18474463..18493676hg19UCSC Ensembl
Innerchr10:18514469..18533682hg18UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3819214
hg1919214
hg1819214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039174
Supporting Variants
Samples
Known GenesCACNB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3507137
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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