A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568612



Internal ID18866893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52609623..52763926hg38UCSC Ensembl
Innerchr17:50686983..50841286hg19UCSC Ensembl
Innerchr17:48041982..48196285hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38154304
hg19154304
hg18154304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065602
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3568612
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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