A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584386



Internal ID20957457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73579269..73579495hg38UCSC Ensembl
chr10:75339027..75339253hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584386
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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