A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540256



Internal ID20913548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101335903..101337047hg38UCSC Ensembl
chr2:101952365..101953509hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg381145
hg191145
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4071n223
Supporting Variantsnssv18255735
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540256
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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