A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516713



Internal ID15444006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:127727525..127755908hg38UCSC Ensembl
Innerchr8:128739771..128768154hg19UCSC Ensembl
Innerchr8:128808953..128837336hg18UCSC Ensembl
Innerchr8:128808953..128837336hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3828384
hg1928384
hg1828384
hg1728384
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688896, nssv702593, nssv680986, nssv690823, nssv672834, nssv687604, nssv695912, nssv674107, nssv670329, nssv655252
Samples
Known GenesMYC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516713
Frequency
Sample Size2026
Observed Gain2
Observed Loss8
Observed Complex0
Frequencyn/a


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