A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152955



Internal ID15877186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161024150..161081425hg38UCSC Ensembl
Innerchr4:161945302..162002577hg19UCSC Ensembl
Innerchr4:162164752..162222027hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3857276
hg1957276
hg1857276
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595924
Supporting Variants
SamplesHGDP00947
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152955
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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