A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3725156



Internal ID19023437
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 StatusS
Merged Variantsnsv1059797
Supporting Variants
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)nssv3725156
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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