A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16905359



Internal ID4385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77324697..77329820hg38UCSC Ensembl
chr1:77790382..77795505hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg385124
hg195124
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554012
Supporting Variants
Samples
Known GenesAK5
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16905359
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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