A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523549



Internal ID21847908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64394510..64397646hg38UCSC Ensembl
chr1:64860193..64863329hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg383137
hg193137
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101719
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523549
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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