A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978886



Internal ID53302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6294000..6300150hg38UCSC Ensembl
chr6:6294233..6300383hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg386151
hg196151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472893
Supporting Variants
Samples
Known GenesF13A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978886
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.010837


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