A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059962



Internal ID19149181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67112871..67149271hg38UCSC Ensembl
Innerchr17:65108987..65145387hg19UCSC Ensembl
Innerchr17:62539449..62575849hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3836401
hg1936401
hg1836401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567741
Samples
Known GenesHELZ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059962
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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