A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029316



Internal ID18771848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:323084..365708hg38UCSC Ensembl
Innerchr6:323084..365708hg19UCSC Ensembl
Innerchr6:268084..310708hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3842625
hg1942625
hg1842625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5897n100
Supporting Variantsnssv3654615
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)nsv1029316
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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