A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061582



Internal ID18804113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43156643..43313710hg38UCSC Ensembl
Innerchr19:43660795..43817862hg19UCSC Ensembl
Innerchr19:48352635..48509702hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38157068
hg19157068
hg18157068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3591n100
Supporting Variantsnssv3574228
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)nsv1061582
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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