A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972646



Internal ID18607862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6012519..6014296hg38UCSC Ensembl
Innerchr9:6012519..6014296hg19UCSC Ensembl
Innerchr9:6002519..6004296hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381778
hg191778
hg181778
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2521936, nssv2521935, nssv2521938, nssv2521941, nssv2521932, nssv2521939, nssv2521940, nssv2521937, nssv2521933, nssv2521934
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRANBP6
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972646
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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