A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171355



Internal ID20738395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76486974..76487514hg38UCSC Ensembl
chr8:77399209..77399749hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419685
Supporting Variants
Samples
Known GenesLINC01111
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171355
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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