A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3574229



Internal ID18525824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43156643..43335547hg38UCSC Ensembl
Innerchr19:43660795..43839699hg19UCSC Ensembl
Innerchr19:48352635..48531539hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38178905
hg19178905
hg18178905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060224
Supporting Variants
Samples
Known GenesLOC284344, PSG4, PSG5, PSG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3574229
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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