A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903204



Internal ID2956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52742922..52869986hg38UCSC Ensembl
chr1:53208594..53335658hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38127065
hg19127065
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556414
Supporting Variants
Samples
Known GenesZYG11A, ZYG11B
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903204
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.004995


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