A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3574226



Internal ID18525821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43154674..43348543hg38UCSC Ensembl
Innerchr19:43658826..43852695hg19UCSC Ensembl
Innerchr19:48350666..48544535hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38193870
hg19193870
hg18193870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058727
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)nssv3574226
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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