A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169727



Internal ID21313538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:118875627..118880840hg38UCSC Ensembl
Outerchr8:118874762..118885079hg38UCSC Ensembl
Innerchr8:119887866..119893079hg19UCSC Ensembl
Outerchr8:119887001..119897318hg19UCSC Ensembl
Innerchr8:119957047..119962260hg18UCSC Ensembl
Outerchr8:119956182..119966499hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3810318
hg1910318
hg1810318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247998
SamplesNGO_11
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169727
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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