A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022544



Internal ID19111762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:153798426..153817988hg38UCSC Ensembl
Innerchr4:154719578..154739140hg19UCSC Ensembl
Innerchr4:154939028..154958590hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3819563
hg1919563
hg1819563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636128
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)nsv1022544
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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