A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3722912



Internal ID19021193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42790226..43026194hg38UCSC Ensembl
Innerchr19:43294378..43530346hg19UCSC Ensembl
Innerchr19:47986218..48222186hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38235969
hg19235969
hg18235969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055674
Supporting Variants
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)nssv3722912
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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