A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689458



Internal ID15079424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58353113..58408935hg38UCSC Ensembl
Innerchr19:58864479..58920302hg19UCSC Ensembl
Innerchr19:63556291..63612114hg18UCSC Ensembl
Innerchr19:63556291..63612114hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3855823
hg1955824
hg1855824
hg1755824
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515731
Supporting Variants
Samples
Known GenesA1BG, A1BG-AS1, LOC646862, MIR4754, RPS5, ZNF497, ZNF584, ZNF837
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689458
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer