A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2524430



Internal ID17784527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21406646..21409788hg38UCSC Ensembl
Innerchr9:21406645..21409787hg19UCSC Ensembl
Innerchr9:21396645..21399787hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg383143
hg193143
hg183143
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968603
Supporting Variants
SamplesHGDP00665
Known GenesIFNA8
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)nssv2524430
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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