A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031208



Internal ID19120429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:267610..360861hg38UCSC Ensembl
Innerchr6:267610..360861hg19UCSC Ensembl
Innerchr6:212610..305861hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3893252
hg1993252
hg1893252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5874n100
Supporting Variantsnssv3653635
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)nsv1031208
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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