A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969670



Internal ID18604897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64406715..64407350hg38UCSC Ensembl
Innerchr9:69419133..69419768hg19UCSC Ensembl
Innerchr9:68708953..68709588hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38636
hg19636
hg18636
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2745720, nssv2745716, nssv2745721, nssv2745723, nssv2745724, nssv2745725, nssv2745717, nssv2745719, nssv2745718, nssv2745722
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A4
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969670
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