A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517391



Internal ID15097998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70632507..70806587hg38UCSC Ensembl
Innerchr16:70666410..70840490hg19UCSC Ensembl
Innerchr16:69223911..69397991hg18UCSC Ensembl
Innerchr16:69223911..69397991hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38174081
hg19174081
hg18174081
hg17174081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683671, nssv687636, nssv688332, nssv692963, nssv661274, nssv685729, nssv673990, nssv661199, nssv655688, nssv703722, nssv651882, nssv688907, nssv692375, nssv652655, nssv653188, nssv668450, nssv666646, nssv659499, nssv666998, nssv680962, nssv665897, nssv690212
Samples
Known GenesIL34, MTSS1L, VAC14, VAC14-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517391
Frequency
Sample Size2026
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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