A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665899



Internal ID15055865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:58305116..58335292hg38UCSC Ensembl
Innerchr17:56382477..56412653hg19UCSC Ensembl
Innerchr17:53737476..53767652hg18UCSC Ensembl
Innerchr17:53737476..53767652hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3830177
hg1930177
hg1830177
hg1730177
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517229
Supporting Variants
Samples
Known GenesBZRAP1, BZRAP1-AS1, MIR142
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665899
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