A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536923



Internal ID20910267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143604894..143606065hg38UCSC Ensembl
chr2:144362463..144363634hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg381172
hg191172
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254489
Samples
Known GenesARHGAP15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536923
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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