A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2522763



Internal ID17531399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21166048..21239961hg38UCSC Ensembl
Innerchr9:21166047..21239960hg19UCSC Ensembl
Innerchr9:21156047..21229960hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3873914
hg1973914
hg1873914
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968599
Supporting Variants
SamplesHGDP01307
Known GenesIFNA10, IFNA14, IFNA16, IFNA17, IFNA21, IFNA4, IFNA7
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)nssv2522763
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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