A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060563



Internal ID19149782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43052691..43105835hg38UCSC Ensembl
Innerchr19:43556843..43609987hg19UCSC Ensembl
Innerchr19:48248683..48301827hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3853145
hg1953145
hg1853145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3586n100
Supporting Variantsnssv3723066
Samples
Known GenesPSG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060563
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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