A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2521938



Internal ID17776655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6012519..6014296hg38UCSC Ensembl
Innerchr9:6012519..6014296hg19UCSC Ensembl
Innerchr9:6002519..6004296hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381778
hg191778
hg181778
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972646
Supporting Variants
SamplesHGDP00542
Known GenesRANBP6
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)nssv2521938
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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