A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547938



Internal ID20921137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51425158..51425899hg38UCSC Ensembl
chr3:51462609..51463350hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260779
Samples
Known GenesVPRBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547938
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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