A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3496247



Internal ID19083888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6612155..6622533hg38UCSC Ensembl
Innerchr10:6654117..6664495hg19UCSC Ensembl
Innerchr10:6694123..6704501hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3810379
hg1910379
hg1810379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055086
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)nssv3496247
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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