A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582204



Internal ID20955275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1644165..1649733hg38UCSC Ensembl
chr10:1686360..1691928hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg385569
hg195569
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218433
Samples
Known GenesADARB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582204
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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