A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220707



Internal ID20787747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95265401..95273600hg38UCSC Ensembl
chr8:96277629..96285828hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424664
Supporting Variants
Samples
Known GenesC8orf37, LOC100616530
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220707
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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