A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169660



Internal ID21313471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97151342..97194942hg38UCSC Ensembl
Outerchr9:97148688..97203276hg38UCSC Ensembl
Innerchr9:99913624..99957224hg19UCSC Ensembl
Outerchr9:99910970..99965558hg19UCSC Ensembl
Innerchr9:98953445..98997045hg18UCSC Ensembl
Outerchr9:98950791..99005379hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3854589
hg1954589
hg1854589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244747
SamplesSNI_10
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169660
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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