A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998828



Internal ID18811678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:70198151..70302146hg38UCSC Ensembl
Innerchr4:71063868..71167863hg19UCSC Ensembl
Innerchr4:71098457..71202452hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38103996
hg19103996
hg18103996
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633074
Samples
Known GenesCSN3, FDCSP, ODAM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998828
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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