A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975969



Internal ID18611176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93943110..93945044hg38UCSC Ensembl
Innerchr11:93676276..93678210hg19UCSC Ensembl
Innerchr11:93315924..93317858hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381935
hg191935
hg181935
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1901876, nssv1901882, nssv1901883, nssv1901885, nssv1901878, nssv1901881, nssv1901880, nssv1901884, nssv1901877, nssv1901879
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)nsv975969
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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