A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539662



Internal ID20912958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:133461334..133621402hg38UCSC Ensembl
chr2:134218905..134378973hg19UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg38160069
hg19160069
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255263
Samples
Known GenesNCKAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539662
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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