A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658576



Internal ID15048542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42817913..43035037hg38UCSC Ensembl
Innerchr19:43322065..43539189hg19UCSC Ensembl
Innerchr19:48013905..48231029hg18UCSC Ensembl
Innerchr19:48013905..48231029hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38217125
hg19217125
hg18217125
hg17217125
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG6, PSG7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658576
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