A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv868949



Internal ID16162905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:22159206..22655796hg38UCSC Ensembl
Innerchr17:21685812..22155123hg19UCSC Ensembl
Innerchr17:21609936..22079250hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38496591
hg19469312
hg18469315
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574610
Supporting Variants
Samples
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv868949
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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