A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2551395



Internal ID17872045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65717292..65719388hg38UCSC Ensembl
Innerchr9:70446657..70448753hg19UCSC Ensembl
Innerchr9:69686477..69688573hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg382097
hg192097
hg182097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv968698
Supporting Variants
SamplesHGDP01284
Known GenesCBWD3, CBWD5
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2551395
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer