A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707680



Internal ID18659275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6453621..6672098hg38UCSC Ensembl
Innerchr10:6495583..6714060hg19UCSC Ensembl
Innerchr10:6535589..6754066hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38218478
hg19218478
hg18218478
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047309
Supporting Variants
Samples
Known GenesPRKCQ, PRKCQ-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3707680
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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