A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv751967



Internal ID16045923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81874595..81875381hg38UCSC Ensembl
Innerchr10:83634351..83635137hg19UCSC Ensembl
Innerchr10:83624331..83625117hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38787
hg19787
hg18787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551689
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)nssv751967
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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