A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596309



Internal ID16383718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:182275371..182308068hg38UCSC Ensembl
Innerchr4:183196524..183229221hg19UCSC Ensembl
Innerchr4:183433518..183466215hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3832698
hg1932698
hg1832698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153267
SamplesHGDP01057
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596309
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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