A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975895



Internal ID18264416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:27887193..27890969hg38UCSC Ensembl
Innerchr11:27908740..27912516hg19UCSC Ensembl
Innerchr11:27865316..27869092hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg383777
hg193777
hg183777
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1879634, nssv1879633, nssv1879636, nssv1879629, nssv1879638, nssv1879637, nssv1879635, nssv1879632, nssv1879631, nssv1879630
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)nsv975895
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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