A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901771



Internal ID1974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43176998..43185765hg38UCSC Ensembl
chr1:43642669..43651436hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg388768
hg198768
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561424
Supporting Variants
Samples
Known GenesWDR65
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901771
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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