A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032709



Internal ID19121931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..322696hg38UCSC Ensembl
Innerchr6:257341..322696hg19UCSC Ensembl
Innerchr6:202341..267696hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3865356
hg1965356
hg1865356
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5882n100
Supporting Variantsnssv3651568, nssv3651565, nssv3651566, nssv3651567, nssv3747622
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)nsv1032709
Frequency
Sample Size11257
Observed Gain1
Observed Loss4
Observed Complex0
Frequencyn/a


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