A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2555609



Internal ID17494512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:83907740..83915531hg38UCSC Ensembl
Innerchr9:86522655..86530446hg19UCSC Ensembl
Innerchr9:85712475..85720266hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg387792
hg197792
hg187792
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972767
Supporting Variants
SamplesHGDP00998
Known GenesKIF27
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)nssv2555609
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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