A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3571668



Internal ID18869949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43001832..43226065hg38UCSC Ensembl
Innerchr19:43505984..43730217hg19UCSC Ensembl
Innerchr19:48197824..48422057hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38224234
hg19224234
hg18224234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061441
Supporting Variants
Samples
Known GenesLOC284344, PSG11, 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)nssv3571668
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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