A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020521



Internal ID19109740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..385772hg38UCSC Ensembl
Innerchr6:264744..385772hg19UCSC Ensembl
Innerchr6:209744..330772hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38121029
hg19121029
hg18121029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3653605, nssv3653603, nssv3653604, nssv3653607, nssv3653606
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)nsv1020521
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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