A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3490875



Internal ID19078516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9913682..10046234hg38UCSC Ensembl
Innerchr10:9955645..10088197hg19UCSC Ensembl
Innerchr10:9995651..10128203hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38132553
hg19132553
hg18132553
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048103
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)nssv3490875
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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