A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024642



Internal ID19113859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..347338hg38UCSC Ensembl
Innerchr6:257341..347338hg19UCSC Ensembl
Innerchr6:202341..292338hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3889998
hg1989998
hg1889998
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5874n100
Supporting Variantsnssv3747627, nssv3651616, nssv3651615, nssv3651614
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)nsv1024642
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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