A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056652



Internal ID19145871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42796042..43026194hg38UCSC Ensembl
Innerchr19:43300194..43530346hg19UCSC Ensembl
Innerchr19:47992034..48222186hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38230153
hg19230153
hg18230153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3558n100
Supporting Variantsnssv3569549
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG6, PSG7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056652
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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