A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557899



Internal ID20930970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177922850..177929510hg38UCSC Ensembl
chr3:177640638..177647298hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg386661
hg196661
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557899
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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