A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575885



Internal ID16363294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66074410..66137608hg38UCSC Ensembl
Innerchr17:64070528..64133726hg19UCSC Ensembl
Innerchr17:61500990..61564188hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3863199
hg1963199
hg1863199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5748n54
Supporting Variantsnssv1149786
SamplesHGDP01325
Known GenesCEP112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575885
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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