A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062391



Internal ID19151610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42795265..43015210hg38UCSC Ensembl
Innerchr19:43299417..43519362hg19UCSC Ensembl
Innerchr19:47991257..48211202hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38219946
hg19219946
hg18219946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3558n100
Supporting Variantsnssv3569524
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)nsv1062391
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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