A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv877272



Internal ID16171228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:83022337..83023022hg38UCSC Ensembl
Innerchr17:80980213..80980898hg19UCSC Ensembl
Innerchr17:78573502..78574187hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38686
hg19686
hg18686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576219
Supporting Variants
Samples
Known GenesB3GNTL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv877272
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer