A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964109



Internal ID18252661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:165404105..165406063hg38UCSC Ensembl
Innerchr4:166325257..166327215hg19UCSC Ensembl
Innerchr4:166544707..166546665hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381959
hg191959
hg181959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2341301, nssv2341299, nssv2341298, nssv2341306, nssv2341304, nssv2341305, nssv2341300, nssv2341297, nssv2341302, nssv2341303
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesCPE
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964109
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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