A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978173



Internal ID18613378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87403122..87403717hg38UCSC Ensembl
Innerchr16:87436728..87437323hg19UCSC Ensembl
Innerchr16:85994229..85994824hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38596
hg19596
hg18596
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2068031, nssv2068831, nssv2068033, nssv2068828, nssv2068034, nssv2068032, nssv2068830, nssv2068030, nssv2068829, nssv2068035
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMAP1LC3B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978173
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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