A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173739



Internal ID20740779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95677453..95692161hg38UCSC Ensembl
chr8:96689681..96704389hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3814709
hg1914709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430478
Supporting Variants
Samples
Known GenesLOC100616530
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173739
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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