A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2524906



Internal ID17874904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21349790..21352301hg38UCSC Ensembl
Innerchr9:21349789..21352300hg19UCSC Ensembl
Innerchr9:21339789..21342300hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg382512
hg192512
hg182512
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968602
Supporting Variants
SamplesHGDP01284
Known GenesIFNA6
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)nssv2524906
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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