A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537253



Internal ID20910592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10713958..10714588hg38UCSC Ensembl
chr2:10854084..10854714hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537253
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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