A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234968



Internal ID20802008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72765738..72765823hg38UCSC Ensembl
chr10:74525496..74525581hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579318
Supporting Variants
Samples
Known GenesMCU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234968
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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