A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2569965



Internal ID17775897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:138231177..138257640hg38UCSC Ensembl
Innerchr9:141121627..141148090hg19UCSC Ensembl
Innerchr9:140241448..140267911hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3826464
hg1926464
hg1826464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968754
Supporting Variants
SamplesHGDP00542
Known GenesFAM157B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2569965
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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