A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17429321



Internal ID22487191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6350681..6355844hg38UCSC Ensembl
chr5:6350794..6355957hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385164
hg195164
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968758
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17429321
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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