A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059797



Internal ID19149016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72830001..72912913hg38UCSC Ensembl
Innerchr17:70826140..70909052hg19UCSC Ensembl
Innerchr17:68337735..68420647hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3882913
hg1982913
hg1882913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725156
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059797
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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