A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062586



Internal ID19151805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:71072937..71135958hg38UCSC Ensembl
Innerchr17:69069078..69132099hg19UCSC Ensembl
Innerchr17:66580673..66643694hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3863022
hg1963022
hg1863022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567765
Samples
Known GenesCASC17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062586
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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