A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705064



Internal ID15095030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4852325..4878596hg38UCSC Ensembl
Innerchr19:4852337..4878608hg19UCSC Ensembl
Innerchr19:4803337..4829608hg18UCSC Ensembl
Innerchr19:4803337..4829608hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3826272
hg1926272
hg1826272
hg1726272
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528462
Supporting Variants
Samples
Known GenesPLIN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705064
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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