A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032862



Internal ID19122084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..365126hg38UCSC Ensembl
Innerchr6:257341..365126hg19UCSC Ensembl
Innerchr6:202341..310126hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38107786
hg19107786
hg18107786
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5880n100
Supporting Variantsnssv3651656, nssv3747633, nssv3651658, nssv3651657
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)nsv1032862
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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