A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269175



Internal ID20836215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64725894..64726358hg38UCSC Ensembl
chr5:64021721..64022185hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570093
Supporting Variants
Samples
Known GenesSREK1IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269175
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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