A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019443



Internal ID19108661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33728487..33793706hg38UCSC Ensembl
Innerchr9:33728485..33793704hg19UCSC Ensembl
Innerchr9:33718485..33783704hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3865220
hg1965220
hg1865220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7518n100
Supporting Variantsnssv3755932
Samples
Known GenesLOC101929688, PRSS3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019443
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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