A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165051



Internal ID20732091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:129797743..129803867hg38UCSC Ensembl
chr8:130809989..130816113hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg386125
hg196125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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