A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011606



Internal ID19100823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:31847601..31970031hg38UCSC Ensembl
Innerchr4:31849223..31971653hg19UCSC Ensembl
Innerchr4:31493121..31615551hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38122431
hg19122431
hg18122431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620639
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)nsv1011606
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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