A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977900



Internal ID18613105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10718802..10726508hg38UCSC Ensembl
Innerchr16:10812659..10820365hg19UCSC Ensembl
Innerchr16:10720160..10727866hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg387707
hg197707
hg187707
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2042837, nssv2042830, nssv2042835, nssv2042833, nssv2042836, nssv2042838, nssv2042834, nssv2042832, nssv2042831, nssv2042839
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977900
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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