A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577946



Internal ID20951017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49366443..49367399hg38UCSC Ensembl
chr17:47443805..47444761hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245137
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577946
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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