A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2369437



Internal ID17744493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97051360..97057102hg38UCSC Ensembl
Innerchr5:96387064..96392806hg19UCSC Ensembl
Innerchr5:96412820..96418562hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg385743
hg195743
hg185743
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968220
Supporting Variants
SamplesHGDP00521
Known Genes
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)nssv2369437
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