A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1106954



Internal ID15960140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16070177..16381359hg38UCSC Ensembl
Innerchr8:15927686..16238868hg19UCSC Ensembl
Innerchr8:15972057..16283239hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38311183
hg19311183
hg18311183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610576
Supporting Variants
Samples
Known GenesMSR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1106954
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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