A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977907



Internal ID18613112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14419292..14424030hg38UCSC Ensembl
Innerchr16:14513149..14517887hg19UCSC Ensembl
Innerchr16:14420650..14425388hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg384739
hg194739
hg184739
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2043346, nssv2043342, nssv2043348, nssv2043349, nssv2043347, nssv2043343, nssv2043344, nssv2043341, nssv2043350, nssv2043345
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)nsv977907
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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