A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869902



Internal ID15817172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36181006..36207778hg38UCSC Ensembl
Innerchr17:34508382..34535178hg19UCSC Ensembl
Innerchr17:31532495..31559291hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3826773
hg1926797
hg1826797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574778
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)nssv869902
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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