A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv988422



Internal ID15935692
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 StatusS
Merged Variantsnsv593328
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv988422
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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