A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572726



Internal ID20945797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99395204..100370143hg38UCSC Ensembl
chr5:98730908..99705847hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38974940
hg19974940
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5835n223
Supporting Variantsnssv18270347
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572726
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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