A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869522



Internal ID15816792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:31142984..31261672hg38UCSC Ensembl
Innerchr17:29470002..29588690hg19UCSC Ensembl
Innerchr17:26494128..26612816hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38118689
hg19118689
hg18118689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574667
Supporting Variants
Samples
Known GenesNF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv869522
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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