A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583721



Internal ID20956792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113887127..113887207hg38UCSC Ensembl
chr10:115646886..115646966hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234409
Samples
Known GenesNHLRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583721
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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