A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550624



Internal ID20923763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101823881..101824556hg38UCSC Ensembl
chr3:101542725..101543400hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38676
hg19676
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259492
Samples
Known GenesNXPE3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550624
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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