A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875903



Internal ID16169859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68084620..68176021hg38UCSC Ensembl
Innerchr17:66080747..66172162hg19UCSC Ensembl
Innerchr17:63592384..63683757hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3891402
hg1991416
hg1891374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575922
Supporting Variants
Samples
Known GenesLINC00674
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv875903
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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