A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981112



Internal ID18616311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26251501..26252117hg38UCSC Ensembl
Innerchr6:26251729..26252345hg19UCSC Ensembl
Innerchr6:26359708..26360324hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38617
hg19617
hg18617
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2397255, nssv2397256, nssv2397261, nssv2397257, nssv2397254, nssv2397263, nssv2397262, nssv2397258, nssv2397260, nssv2397259
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHIST1H2BH
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981112
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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