A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576932



Internal ID20950003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4165485..4166229hg38UCSC Ensembl
chr10:4207677..4208421hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38745
hg19745
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220660
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576932
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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