A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581941



Internal ID20955012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37954673..37955806hg38UCSC Ensembl
chr10:38243601..38244734hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg381134
hg191134
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223548
Samples
Known GenesZNF25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581941
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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