A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169375



Internal ID21313858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92560356..92575238hg38UCSC Ensembl
Outerchr9:92548404..92575886hg38UCSC Ensembl
Innerchr9:95322638..95337520hg19UCSC Ensembl
Outerchr9:95310686..95338168hg19UCSC Ensembl
Innerchr9:94362459..94377341hg18UCSC Ensembl
Outerchr9:94350507..94377989hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3827483
hg1927483
hg1827483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247734
SamplesMLY_8
Known GenesCENPP
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169375
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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