A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972787



Internal ID18261317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:95293068..95294753hg38UCSC Ensembl
Innerchr9:98055350..98057035hg19UCSC Ensembl
Innerchr9:97095171..97096856hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381686
hg191686
hg181686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2559597, nssv2559590, nssv2559598, nssv2559596, nssv2559589, nssv2559591, nssv2559593, nssv2559592, nssv2559595, nssv2559594
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFANCC
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972787
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