A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562131



Internal ID20935202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3984487..4019640hg38UCSC Ensembl
chr5:3984601..4019754hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3835154
hg1935154
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268334
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562131
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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