A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035024



Internal ID19124243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33728487..33798190hg38UCSC Ensembl
Innerchr9:33728485..33798188hg19UCSC Ensembl
Innerchr9:33718485..33788188hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3869704
hg1969704
hg1869704
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7518n100
Supporting Variantsnssv3688879
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)nsv1035024
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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