A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173861



Internal ID15855219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:23512626..23580246hg38UCSC Ensembl
Innerchr10:23801555..23869175hg19UCSC Ensembl
Innerchr10:23841561..23909181hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3867621
hg1967621
hg1867621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550215
Supporting Variants
Samples1780862487_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173861
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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