A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965756



Internal ID18254300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:113861243..113862546hg38UCSC Ensembl
Innerchr6:114182421..114183723hg19UCSC Ensembl
Innerchr6:114289114..114290416hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381304
hg191303
hg181303
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2421009, nssv2421005, nssv2421007, nssv2421002, nssv2421003, nssv2421004, nssv2421010, nssv2421006, nssv2421008, nssv2421001
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMARCKS
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965756
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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