A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064219



Internal ID19153438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43037255..43249346hg38UCSC Ensembl
Innerchr19:43541407..43753498hg19UCSC Ensembl
Innerchr19:48233247..48445338hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38212092
hg19212092
hg18212092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3585n100
Supporting Variantsnssv3571758, nssv3571756, nssv3571759, nssv3571757
Samples
Known GenesLOC284344, PSG2, PSG4, PSG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064219
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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