A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058727



Internal ID18801258
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 StatusM
Merged Variantsdgv3591n100
Supporting Variantsnssv3574226, nssv3574225
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)nsv1058727
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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