A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2560175



Internal ID17875671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96407251..96409605hg38UCSC Ensembl
Innerchr9:99169533..99171887hg19UCSC Ensembl
Innerchr9:98209354..98211708hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg382355
hg192355
hg182355
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968736
Supporting Variants
SamplesHGDP01284
Known GenesZNF367
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)nssv2560175
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