A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542455



Internal ID20915714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15690634..15692084hg38UCSC Ensembl
chr3:15732141..15733591hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381451
hg191451
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261037
Samples
Known GenesANKRD28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542455
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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