A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv959943



Internal ID18595199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:90223164..90228345hg38UCSC Ensembl
Innerchr16:90289572..90294753hg19UCSC Ensembl
Innerchr16:88817073..88822561hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg385182
hg195182
hg185489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2652150, nssv2652149, nssv2652152, nssv2652151, nssv2652147, nssv2652154, nssv2652155, nssv2652156, nssv2652148, nssv2652153
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv959943
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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