A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972754



Internal ID18261284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68298799..68342297hg38UCSC Ensembl
Innerchr9:70913715..70957213hg19UCSC Ensembl
Innerchr9:70103535..70147033hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3843499
hg1943499
hg1843499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2552023, nssv2552026, nssv2552018, nssv2552024, nssv2552025, nssv2552019, nssv2552022, nssv2552021, nssv2552017, nssv2552020
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCBWD3, FOXD4L3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972754
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