A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542184



Internal ID20915448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36897068..36897774hg38UCSC Ensembl
chr2:37124211..37124917hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260165
Samples
Known GenesSTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542184
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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