A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174148



Internal ID15855049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20489512..20525654hg38UCSC Ensembl
Innerchr10:20778441..20814583hg19UCSC Ensembl
Innerchr10:20818447..20854589hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3836143
hg1936143
hg1836143
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550151
Supporting Variants
Samples1780862431_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174148
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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