A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980235



Internal ID18615435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102662072..102663592hg38UCSC Ensembl
Innerchr4:103583229..103584749hg19UCSC Ensembl
Innerchr4:103802277..103803797hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381521
hg191521
hg181521
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2329493, nssv2329494, nssv2329496, nssv2329495, nssv2329487, nssv2329489, nssv2329490, nssv2329491, nssv2329488, nssv2329492
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMANBA
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980235
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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