A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972653



Internal ID18607869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21811295..21811795hg38UCSC Ensembl
Innerchr9:21811294..21811794hg19UCSC Ensembl
Innerchr9:21801294..21801794hg18UCSC Ensembl
Cytoband9p21.3
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 Variantsnssv2525822, nssv2525820, nssv2525826, nssv2525821, nssv2525824, nssv2525825, nssv2525823, nssv2525818, nssv2525827, nssv2525819
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMTAP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972653
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