A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596308



Internal ID16383717
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 StatusM
Merged Variants
Supporting Variantsnssv1153266
SamplesHGDP00023
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596308
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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