A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701043



Internal ID15091009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58387069..58434689hg38UCSC Ensembl
Innerchr19:58898436..58946056hg19UCSC Ensembl
Innerchr19:63590248..63637868hg18UCSC Ensembl
Innerchr19:63590248..63637868hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3847621
hg1947621
hg1847621
hg1747621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515731
Supporting Variants
Samples
Known GenesLOC646862, RPS5, ZNF132, ZNF584
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701043
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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