A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575962



Internal ID16363371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72807479..72823658hg38UCSC Ensembl
Innerchr17:70803618..70819797hg19UCSC Ensembl
Innerchr17:68315213..68331392hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3816180
hg1916180
hg1816180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5763n54
Supporting Variantsnssv875939
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575962
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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