A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026960



Internal ID19116178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..315197hg38UCSC Ensembl
Innerchr6:257341..315197hg19UCSC Ensembl
Innerchr6:202341..260197hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3857857
hg1957857
hg1857857
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5882n100
Supporting Variantsnssv3747609, nssv3651538, nssv3651540, nssv3651541, nssv3651542, nssv3651539, nssv3747610, nssv3747608, nssv3651537
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)nsv1026960
Frequency
Sample Size11257
Observed Gain5
Observed Loss4
Observed Complex0
Frequencyn/a


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