A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044171



Internal ID19133390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:113428389..113471711hg38UCSC Ensembl
Innerchr10:115188148..115231470hg19UCSC Ensembl
Innerchr10:115178138..115221460hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3843323
hg1943323
hg1843323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513952
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)nsv1044171
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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