A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575968



Internal ID16016691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72819272..72821975hg38UCSC Ensembl
Innerchr17:70815411..70818114hg19UCSC Ensembl
Innerchr17:68327006..68329709hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg382704
hg192704
hg182704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5764n54
Supporting Variantsnssv875953, nssv875954, nssv875956, nssv875951, nssv875957, nssv875952, nssv875955, nssv875958, nssv875950, nssv875959
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575968
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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