A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975218



Internal ID18610426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:92160689..92161981hg38UCSC Ensembl
Innerchr11:91893855..91895147hg19UCSC Ensembl
Innerchr11:91533503..91534795hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg381293
hg191293
hg181293
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1900968, nssv1900963, nssv1900961, nssv1900965, nssv1900967, nssv1900970, nssv1900966, nssv1900962, nssv1900969, nssv1900964
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)nsv975218
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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