A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869901



Internal ID15817171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36180353..36206928hg38UCSC Ensembl
Innerchr17:34507719..34534328hg19UCSC Ensembl
Innerchr17:31531832..31558441hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3826576
hg1926610
hg1826610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574777
Supporting Variants
Samples
Known GenesCCL3L1, CCL3L3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv869901
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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