A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034170



Internal ID19123392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..316401hg38UCSC Ensembl
Innerchr6:264744..316401hg19UCSC Ensembl
Innerchr6:209744..261401hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3851658
hg1951658
hg1851658
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5882n100
Supporting Variantsnssv3653554, nssv3747782, nssv3747783, nssv3653555, nssv3653556
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)nsv1034170
Frequency
Sample Size11257
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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