A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576960



Internal ID20950031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45523743..45552409hg38UCSC Ensembl
chr10:46019191..46047857hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3828667
hg1928667
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229801
Samples
Known GenesMARCH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576960
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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