A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969546



Internal ID18604773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40243697..40244197hg38UCSC Ensembl
Innerchr9:42388715..42389215hg19UCSC Ensembl
Innerchr9:42378711..42379211hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2728230, nssv2728172, nssv2728236, nssv2728177, nssv2728232, nssv2728175, nssv2728170, nssv2728178, nssv2728169, nssv2728231, nssv2728234, nssv2728229, nssv2728227, nssv2728171, nssv2728176, nssv2728233, nssv2728174, nssv2728235, nssv2728228, nssv2728173
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969546
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