A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037953



Internal ID19127172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130472908..130500681hg38UCSC Ensembl
Innerchr10:132271172..132298945hg19UCSC Ensembl
Innerchr10:132161162..132188935hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3827774
hg1927774
hg1827774
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706258
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)nsv1037953
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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