A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971649



Internal ID18606866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:47157173..47167299hg38UCSC Ensembl
Innerchr8:48068796..48078922hg19UCSC Ensembl
Innerchr8:48187961..48198087hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3810127
hg1910127
hg1810127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2501895, nssv2501896, nssv2501887, nssv2501888, nssv2501889, nssv2501890, nssv2501894, nssv2501893, nssv2501891, nssv2501892
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)nsv971649
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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