A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019316



Internal ID19108534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:253861..349386hg38UCSC Ensembl
Innerchr6:253861..349386hg19UCSC Ensembl
Innerchr6:198861..294386hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3895526
hg1995526
hg1895526
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5874n100
Supporting Variantsnssv3746770
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)nsv1019316
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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