A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011566



Internal ID19100783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62982908..63289108hg38UCSC Ensembl
Innerchr4:63848626..64154826hg19UCSC Ensembl
Innerchr4:63531221..63837421hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38306201
hg19306201
hg18306201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5223n100
Supporting Variantsnssv3626530
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011566
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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