A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2548155



Internal ID17806411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63110185..63202862hg38UCSC Ensembl
Innerchr9:67015157..67107834hg19UCSC Ensembl
Innerchr9:66754977..66847905hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3892678
hg1992678
hg1892929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv982281
Supporting Variants
SamplesHGDP00778
Known GenesLOC286297
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)nssv2548155
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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