A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033176



Internal ID19122398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:254255..294462hg38UCSC Ensembl
Innerchr6:254255..294462hg19UCSC Ensembl
Innerchr6:199255..239462hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3840208
hg1940208
hg1840208
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5881n100
Supporting Variantsnssv3650421, nssv3650422
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)nsv1033176
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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