A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv868782



Internal ID15816052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16491673..16492312hg38UCSC Ensembl
Innerchr17:16394987..16395626hg19UCSC Ensembl
Innerchr17:16335712..16336351hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38640
hg19640
hg18640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574491
Supporting Variants
Samples
Known GenesFAM211A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv868782
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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