A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588127



Internal ID20961198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50931262..50932054hg38UCSC Ensembl
chr15:51223459..51224251hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38793
hg19793
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2536n223
Supporting Variantsnssv18240325
Samples
Known GenesAP4E1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588127
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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