A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152957



Internal ID15880093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161024150..161082472hg38UCSC Ensembl
Innerchr4:161945302..162003624hg19UCSC Ensembl
Innerchr4:162164752..162223074hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3858323
hg1958323
hg1858323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595925
Supporting Variants
SamplesNINDS_155
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152957
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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