A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581331



Internal ID20954402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99933850..99962582hg38UCSC Ensembl
chr10:101693607..101722339hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3828733
hg1928733
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227649
Samples
Known GenesDNMBP, DNMBP-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581331
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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