A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972300



Internal ID18260830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21367213..21369886hg38UCSC Ensembl
Innerchr9:21367212..21369885hg19UCSC Ensembl
Innerchr9:21357212..21359885hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg382674
hg192674
hg182674
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2525006, nssv2525000, nssv2524999, nssv2525007, nssv2525008, nssv2525005, nssv2525003, nssv2525004, nssv2525001, nssv2525002
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesIFNA13
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972300
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