A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575961



Internal ID16363370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72807479..72822670hg38UCSC Ensembl
Innerchr17:70803618..70818809hg19UCSC Ensembl
Innerchr17:68315213..68330404hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3815192
hg1915192
hg1815192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5763n54
Supporting Variantsnssv875938, nssv875937
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575961
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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