A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537265



Internal ID20910603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:230150940..230151637hg38UCSC Ensembl
chr2:231015656..231016353hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38698
hg19698
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257290
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537265
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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