A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055674



Internal ID19144893
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 StatusM
Merged Variantsdgv3558n100
Supporting Variantsnssv3571636, nssv3722913, nssv3722912, nssv3571635, nssv3571637
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)nsv1055674
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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