A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562891



Internal ID20935962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65694369..65694591hg38UCSC Ensembl
chr5:64990196..64990418hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269194
Samples
Known GenesSGTB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562891
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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