A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964097



Internal ID18599335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134951564..134953272hg38UCSC Ensembl
Innerchr4:135872719..135874427hg19UCSC Ensembl
Innerchr4:136092169..136093877hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg381709
hg191709
hg181709
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2335976, nssv2335979, nssv2335982, nssv2335984, nssv2335977, nssv2335978, nssv2335980, nssv2335981, nssv2335983, nssv2335985
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)nsv964097
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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