A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901564



Internal ID1847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40510999..40517400hg38UCSC Ensembl
chr1:40976671..40983072hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg386402
hg196402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425169
Supporting Variants
Samples
Known GenesEXO5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901564
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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