A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv868819



Internal ID15816089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16784966..16814911hg38UCSC Ensembl
Innerchr17:16688280..16718225hg19UCSC Ensembl
Innerchr17:16629005..16658950hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3829946
hg1929946
hg1829946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574504
Supporting Variants
Samples
Known GenesFAM106CP, USP32P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv868819
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