A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032952



Internal ID19122174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:180186867..180227529hg38UCSC Ensembl
Innerchr4:181108020..181148682hg19UCSC Ensembl
Innerchr4:181345014..181385676hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3840663
hg1940663
hg1840663
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635570
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)nsv1032952
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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