A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964089



Internal ID18599327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:118642826..118671305hg38UCSC Ensembl
Innerchr4:119563981..119592460hg19UCSC Ensembl
Innerchr4:119783429..119811908hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3828480
hg1928480
hg1828480
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2334388, nssv2334395, nssv2334386, nssv2334393, nssv2334391, nssv2334394, nssv2334389, nssv2334392, nssv2334390, nssv2334387
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964089
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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