A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149351



Internal ID15873612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:22203657..22530697hg38UCSC Ensembl
Innerchr17:21730263..22030023hg19UCSC Ensembl
Innerchr17:21654390..21954150hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38327041
hg19299761
hg18299761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574613
Supporting Variants
SamplesHGDP00264
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149351
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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