A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517320



Internal ID15444613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85264081..85276284hg38UCSC Ensembl
Innerchr16:85297687..85309890hg19UCSC Ensembl
Innerchr16:83855188..83867391hg18UCSC Ensembl
Innerchr16:83855188..83867391hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3812204
hg1912204
hg1812204
hg1712204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686677, nssv662295, nssv678967, nssv684884, nssv659244, nssv653407, nssv688836, nssv687691, nssv692093, nssv658047, nssv687546, nssv677404, nssv651704, nssv670553, nssv690629, nssv691693, nssv659143, nssv675844, nssv690602, nssv668490, nssv678122, nssv691582, nssv665387, nssv662986, nssv680110, nssv670956, nssv653079, nssv670311, nssv677374, nssv669724, nssv652393, nssv682625, nssv703281, nssv666235
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517320
Frequency
Sample Size2026
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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