A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059112



Internal ID19148331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42882021..43020166hg38UCSC Ensembl
Innerchr19:43386173..43524318hg19UCSC Ensembl
Innerchr19:48078013..48216158hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38138146
hg19138146
hg18138146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3575n100
Supporting Variantsnssv3570145, nssv3570146
Samples
Known GenesPSG11, PSG6, PSG7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059112
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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