A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543568



Internal ID20916814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202288547..202290106hg38UCSC Ensembl
chr2:203153270..203154829hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381560
hg191560
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4255n223
Supporting Variantsnssv18257705
Samples
Known GenesNOP58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543568
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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