A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017073



Internal ID18759608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:323084..364575hg38UCSC Ensembl
Innerchr6:323084..364575hg19UCSC Ensembl
Innerchr6:268084..309575hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3841492
hg1941492
hg1841492
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5897n100
Supporting Variantsnssv3654614, nssv3653875
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)nsv1017073
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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