A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972377



Internal ID18607593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62884949..62898311hg38UCSC Ensembl
Innerchr9:66540773..66554135hg19UCSC Ensembl
Innerchr9:66280593..66293955hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3813363
hg1913363
hg1813363
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2547844, nssv2547848, nssv2547842, nssv2547850, nssv2547845, nssv2547843, nssv2547841, nssv2547846, nssv2547847, nssv2547849
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMGC21881
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972377
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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