A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969356



Internal ID18604583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26199671..26204165hg38UCSC Ensembl
Innerchr6:26199899..26204393hg19UCSC Ensembl
Innerchr6:26307878..26312372hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg384495
hg194495
hg184495
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2396428, nssv2396429, nssv2396421, nssv2396422, nssv2396420, nssv2396425, nssv2396426, nssv2396427, nssv2396424, nssv2396423
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHIST1H2BF
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969356
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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