A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153266



Internal ID15872723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:182200078..182216459hg38UCSC Ensembl
Innerchr4:183121231..183137612hg19UCSC Ensembl
Innerchr4:183358225..183374606hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3816382
hg1916382
hg1816382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596308
Supporting Variants
SamplesHGDP00023
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153266
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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