A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015323



Internal ID18757857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..389630hg38UCSC Ensembl
Innerchr6:257341..389630hg19UCSC Ensembl
Innerchr6:202341..334630hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38132290
hg19132290
hg18132290
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5872n100
Supporting Variantsnssv3652670, nssv3652669, nssv3652671
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015323
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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