A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547838



Internal ID20921038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44497745..44498087hg38UCSC Ensembl
chr3:44539237..44539579hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547838
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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