A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869992



Internal ID15817262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36212480..36247042hg38UCSC Ensembl
Innerchr17:34539882..34574488hg19UCSC Ensembl
Innerchr17:31563995..31598601hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3834563
hg1934607
hg1834607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574811
Supporting Variants
Samples
Known GenesCCL4L1, CCL4L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv869992
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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