A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575877



Internal ID16363286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:65946135..66098393hg38UCSC Ensembl
Innerchr17:63942253..64094511hg19UCSC Ensembl
Innerchr17:61372715..61524973hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38152259
hg19152259
hg18152259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5747n54
Supporting Variantsnssv875823
Samples
Known GenesCEP112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575877
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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