A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975971



Internal ID18264492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94757667..94759204hg38UCSC Ensembl
Innerchr11:94490833..94492370hg19UCSC Ensembl
Innerchr11:94130481..94132018hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381538
hg191538
hg181538
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1902021, nssv1902027, nssv1902023, nssv1902024, nssv1902026, nssv1902025, nssv1902022, nssv1902028, nssv1902020, nssv1902029
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)nsv975971
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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