A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593328



Internal ID16034051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1601262..1625429hg38UCSC Ensembl
Innerchr4:1602989..1627156hg19UCSC Ensembl
Innerchr4:1572949..1597115hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3824168
hg1924168
hg1824167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8900n54
Supporting Variantsnssv988422
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593328
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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