A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516905



Internal ID18815186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15876551..15889061hg38UCSC Ensembl
Innerchr10:15918550..15931060hg19UCSC Ensembl
Innerchr10:15958556..15971066hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3812511
hg1912511
hg1812511
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036279
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)nssv3516905
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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