A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593089



Internal ID20966160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37958916..37959803hg38UCSC Ensembl
chr10:38247844..38248731hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38888
hg19888
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236548
Samples
Known GenesZNF25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593089
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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