A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582385



Internal ID20955456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75151699..75152468hg38UCSC Ensembl
chr10:76911457..76912226hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225038
Samples
Known GenesSAMD8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582385
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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