A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594644



Internal ID16382053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:70115421..70201600hg38UCSC Ensembl
Innerchr4:70981138..71067317hg19UCSC Ensembl
Innerchr4:71015727..71101906hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3886180
hg1986180
hg1886180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9126n54
Supporting Variantsnssv1002277
Samples
Known GenesC4orf40, CSN1S2BP, ODAM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594644
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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