A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169681



Internal ID21313492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57450745..57479376hg38UCSC Ensembl
Outerchr10:57443289..57482162hg38UCSC Ensembl
Innerchr10:59210505..59239136hg19UCSC Ensembl
Outerchr10:59203049..59241922hg19UCSC Ensembl
Innerchr10:58880511..58909142hg18UCSC Ensembl
Outerchr10:58873055..58911928hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3838874
hg1938874
hg1838874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244279
SamplesSNI_9
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169681
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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