A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974795



Internal ID18610004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:29482470..29521497hg38UCSC Ensembl
Innerchr16:29493791..29532818hg19UCSC Ensembl
Innerchr16:29401292..29440319hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3839028
hg1939028
hg1839028
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2054790, nssv2054796, nssv2054794, nssv2054798, nssv2054792, nssv2054793, nssv2054789, nssv2054791, nssv2054797, nssv2054795
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)nsv974795
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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