A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2297964



Internal ID17754730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177623664..177624386hg38UCSC Ensembl
Innerchr3:177341452..177342174hg19UCSC Ensembl
Innerchr3:178824146..178824868hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38723
hg19723
hg18723
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv963381
Supporting Variants
SamplesHGDP00521
Known GenesLINC00578
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)nssv2297964
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