A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969367



Internal ID18604594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27838096..27839734hg38UCSC Ensembl
Innerchr6:27805874..27807512hg19UCSC Ensembl
Innerchr6:27913853..27915491hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381639
hg191639
hg181639
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2399957, nssv2399956, nssv2399963, nssv2399959, nssv2399964, nssv2399955, nssv2399962, nssv2399961, nssv2399958, nssv2399960
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHIST1H2AK, HIST1H2BN
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969367
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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