A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2570403



Internal ID17853387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135519952..135526968hg38UCSC Ensembl
Innerchr9:138411798..138418814hg19UCSC Ensembl
Innerchr9:137551619..137558635hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg387017
hg197017
hg187017
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972463
Supporting Variants
SamplesHGDP01029
Known GenesLCN1
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)nssv2570403
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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