A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554602



Internal ID20927696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202181076..202181436hg38UCSC Ensembl
chr2:203045799..203046159hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256407
Samples
Known GenesLOC100652824
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554602
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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