A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595004



Internal ID16382413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:103886001..104133831hg38UCSC Ensembl
Innerchr4:104807158..105054988hg19UCSC Ensembl
Innerchr4:105026607..105274437hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38247831
hg19247831
hg18247831
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1003692
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595004
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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