A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892987



Internal ID169485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178526150..178526503hg38UCSC Ensembl
chr1:178495285..178495638hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139387
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892987
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.13862


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