A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973207



Internal ID18608422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33572281..33576350hg38UCSC Ensembl
Innerchr9:33572279..33576348hg19UCSC Ensembl
Innerchr9:33562279..33566348hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg384070
hg194070
hg184070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2722983, nssv2722986, nssv2722984, nssv2722981, nssv2722985, nssv2722979, nssv2722987, nssv2722988, nssv2722980, nssv2722982
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD18B
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973207
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