A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2560904



Internal ID17531125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93564348..93565557hg38UCSC Ensembl
Innerchr9:96326630..96327839hg19UCSC Ensembl
Innerchr9:95366451..95367660hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381210
hg191210
hg181210
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968731
Supporting Variants
SamplesHGDP01307
Known GenesFAM120A
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)nssv2560904
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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