A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033868



Internal ID19123089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9901840..9929797hg38UCSC Ensembl
Innerchr5:9901952..9929909hg19UCSC Ensembl
Innerchr5:9954952..9982909hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3827958
hg1927958
hg1827958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5566n100
Supporting Variantsnssv3748673, nssv3638179
Samples
Known GenesLOC285692
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033868
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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