A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554620



Internal ID20927714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206070667..206071285hg38UCSC Ensembl
chr2:206935391..206936009hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258507
Samples
Known GenesINO80D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554620
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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