A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891098



Internal ID168242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149656000..149674600hg38UCSC Ensembl
chr1:149627610..149646169hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3818601
hg1918560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138445
Supporting Variants
Samples
Known GenesLINC00869
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891098
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.045179


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