A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170974



Internal ID20738014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8749655..8933105hg38UCSC Ensembl
chr8:8607165..8790615hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38183451
hg19183451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425274
Supporting Variants
Samples
Known GenesMFHAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170974
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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