A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964079



Internal ID18599317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:108621771..108623750hg38UCSC Ensembl
Innerchr4:109542927..109544906hg19UCSC Ensembl
Innerchr4:109762376..109764355hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381980
hg191980
hg181980
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2329651, nssv2329655, nssv2329659, nssv2329650, nssv2329656, nssv2329654, nssv2329653, nssv2329657, nssv2329658, nssv2329652
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRPL34
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964079
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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