A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869521



Internal ID16163477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:30862812..30886925hg38UCSC Ensembl
Innerchr17:29189830..29213943hg19UCSC Ensembl
Innerchr17:26213956..26238069hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3824114
hg1924114
hg1824114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574666
Supporting Variants
Samples
Known GenesATAD5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv869521
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