A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587687



Internal ID20960758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37959633..37960624hg38UCSC Ensembl
chr10:38248561..38249552hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38992
hg19992
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233104
Samples
Known GenesZNF25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587687
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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