A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162977



Internal ID20730019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:112235601..112236400hg38UCSC Ensembl
chr8:113247830..113248629hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419542
Supporting Variants
Samples
Known GenesCSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162977
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00042


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