A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527898



Internal ID15455191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52437059..52585995hg38UCSC Ensembl
Innerchr17:50514419..50663355hg19UCSC Ensembl
Innerchr17:47869418..48018354hg18UCSC Ensembl
Innerchr17:47869418..48018354hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38148937
hg19148937
hg18148937
hg17148937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704402
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527898
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