A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514691



Internal ID18812972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19031041..19055881hg38UCSC Ensembl
Innerchr10:19319970..19344810hg19UCSC Ensembl
Innerchr10:19359976..19384816hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3824841
hg1924841
hg1824841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043004
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3514691
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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