A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869994



Internal ID15817264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36213557..36241868hg38UCSC Ensembl
Innerchr17:34541011..34569314hg19UCSC Ensembl
Innerchr17:31565124..31593427hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3828312
hg1928304
hg1828304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574813
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv869994
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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