A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060996



Internal ID19150215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42978561..43132427hg38UCSC Ensembl
Innerchr19:43482713..43636579hg19UCSC Ensembl
Innerchr19:48174553..48328419hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38153867
hg19153867
hg18153867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3581n100
Supporting Variantsnssv3570195
Samples
Known GenesPSG11, PSG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060996
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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