A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007196



Internal ID18749727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46767886..46838650hg38UCSC Ensembl
Innerchr3:46809376..46880140hg19UCSC Ensembl
Innerchr3:46784380..46855144hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3870765
hg1970765
hg1870765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4732n100
Supporting Variantsnssv3595227
Samples
Known GenesPRSS42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007196
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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