A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062414



Internal ID19151633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33984009..34054392hg38UCSC Ensembl
Innerchr17:32311028..32381411hg19UCSC Ensembl
Innerchr17:29335141..29405524hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3870384
hg1970384
hg1870384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3561066
Samples
Known GenesASIC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062414
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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