A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585041



Internal ID20958112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49537335..49537719hg38UCSC Ensembl
chr10:50745381..50745765hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226913
Samples
Known GenesERCC6, ERCC6-PGBD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585041
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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