A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023739



Internal ID19112956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..343132hg38UCSC Ensembl
Innerchr6:257341..343132hg19UCSC Ensembl
Innerchr6:202341..288132hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3885792
hg1985792
hg1885792
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5874n100
Supporting Variantsnssv3651610, nssv3651609
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)nsv1023739
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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