A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548637



Internal ID20921821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24598623..24599180hg38UCSC Ensembl
chr1:24925114..24925671hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv127n223
Supporting Variantsnssv18251455
Samples
Known GenesNCMAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548637
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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