A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595754



Internal ID16383163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:154850479..154871812hg38UCSC Ensembl
Innerchr4:155771631..155792964hg19UCSC Ensembl
Innerchr4:155991081..156012414hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3821334
hg1921334
hg1821334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153184
SamplesHGDP00553
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595754
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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