A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596192



Internal ID16383601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:171462288..171560040hg38UCSC Ensembl
Innerchr4:172383439..172481191hg19UCSC Ensembl
Innerchr4:172620014..172717766hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3897753
hg1997753
hg1897753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9389n54
Supporting Variantsnssv1014360
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596192
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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