A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752121



Internal ID16046077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82741762..82797819hg38UCSC Ensembl
Innerchr10:84501518..84557575hg19UCSC Ensembl
Innerchr10:84491498..84547555hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3856058
hg1956058
hg1856058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551736
Supporting Variants
Samples
Known GenesNRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv752121
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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