A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541705



Internal ID20914987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202268258..202268844hg38UCSC Ensembl
chr2:203132981..203133567hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256417
Samples
Known GenesNOP58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541705
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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