A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16897485



Internal ID172475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227990281..228026837hg38UCSC Ensembl
chr1:228177982..228214538hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3836557
hg1936557
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563296
Supporting Variants
Samples
Known GenesWNT3A
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16897485
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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