A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866440



Internal ID16160396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:2694675..2764987hg38UCSC Ensembl
Innerchr17:2597969..2668281hg19UCSC Ensembl
Innerchr17:2544719..2615031hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3870313
hg1970313
hg1870313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574225
Supporting Variants
Samples
Known GenesCLUH, MIR1253
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866440
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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