A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972777



Internal ID18607993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88322918..88332059hg38UCSC Ensembl
Innerchr9:90937833..90946974hg19UCSC Ensembl
Innerchr9:90127653..90136794hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg389142
hg199142
hg189142
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2558187, nssv2558185, nssv2558190, nssv2558188, nssv2558181, nssv2558182, nssv2558186, nssv2558189, nssv2558183, nssv2558184
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972777
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