A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543016



Internal ID20916267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15273926..15274800hg38UCSC Ensembl
chr2:15414050..15414924hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254628
Samples
Known GenesNBAS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543016
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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