A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574397



Internal ID20947468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24530422..24531182hg38UCSC Ensembl
chr4:24532045..24532805hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265610
Samples
Known GenesDHX15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574397
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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