A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971668



Internal ID18606885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:75302034..75304028hg38UCSC Ensembl
Innerchr8:76214269..76216263hg19UCSC Ensembl
Innerchr8:76376824..76378818hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381995
hg191995
hg181995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2508850, nssv2508852, nssv2508843, nssv2508847, nssv2508844, nssv2508851, nssv2508845, nssv2508848, nssv2508846, nssv2508849
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCASC9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971668
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer