A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269138



Internal ID20836178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:62313806..62314376hg38UCSC Ensembl
chr5:61609633..61610203hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572280
Supporting Variants
Samples
Known GenesKIF2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269138
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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