A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969366



Internal ID18257907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27807410..27808693hg38UCSC Ensembl
Innerchr6:27775188..27776471hg19UCSC Ensembl
Innerchr6:27883167..27884450hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381284
hg191284
hg181284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2398971, nssv2398974, nssv2398976, nssv2398978, nssv2398972, nssv2398977, nssv2398970, nssv2398973, nssv2398975, nssv2398969
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesHIST1H2AI, HIST1H2BL
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969366
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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