A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032555



Internal ID19121777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189764797..189920867hg38UCSC Ensembl
Innerchr4:190685951..190842022hg19UCSC Ensembl
Innerchr4:190922945..191079016hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38156071
hg19156072
hg18156072
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744556
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)nsv1032555
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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