A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021947



Internal ID19111165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..302294hg38UCSC Ensembl
Innerchr6:264744..302294hg19UCSC Ensembl
Innerchr6:209744..247294hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3837551
hg1937551
hg1837551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5886n100
Supporting Variantsnssv3653540, nssv3653541
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)nsv1021947
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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