A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574667



Internal ID16015390
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 StatusM
Merged Variants
Supporting Variantsnssv869522
Samples
Known GenesNF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574667
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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