A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664005



Internal ID15400657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53639597..53644791hg38UCSC Ensembl
Innerchr19:54142851..54148045hg19UCSC Ensembl
Innerchr19:58834663..58839857hg18UCSC Ensembl
Innerchr19:58834663..58839857hg17UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg385195
hg195195
hg185195
hg175195
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515586
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664005
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