A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265616



Internal ID20832656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24825663..24825959hg38UCSC Ensembl
chr4:24827285..24827581hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566114
Supporting Variants
Samples
Known GenesCCDC149
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265616
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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