A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv877116



Internal ID15824386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81526313..81537989hg38UCSC Ensembl
Innerchr17:79493339..79505015hg19UCSC Ensembl
Innerchr17:77107934..77115491hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3811677
hg1911677
hg187558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576181
Supporting Variants
Samples
Known GenesFSCN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv877116
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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