A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061598



Internal ID18804129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42733612..42911560hg38UCSC Ensembl
Innerchr19:43237764..43415712hg19UCSC Ensembl
Innerchr19:47929604..48107552hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38177949
hg19177949
hg18177949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3552n100
Supporting Variantsnssv3568675
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG3, PSG6, PSG8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061598
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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