A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981197



Internal ID18269710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151224744..151225960hg38UCSC Ensembl
Innerchr6:151545879..151547095hg19UCSC Ensembl
Innerchr6:151587572..151588788hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381217
hg191217
hg181217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2427206, nssv2427213, nssv2427210, nssv2427209, nssv2427212, nssv2427207, nssv2427214, nssv2427211, nssv2427208, nssv2427205
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981197
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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