A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667897



Internal ID15057863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42870449..43001832hg38UCSC Ensembl
Innerchr19:43374601..43505984hg19UCSC Ensembl
Innerchr19:48066441..48197824hg18UCSC Ensembl
Innerchr19:48066441..48197824hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38131384
hg19131384
hg18131384
hg17131384
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesPSG1, PSG6, PSG7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667897
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