A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549172



Internal ID20922340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143631303..143631485hg38UCSC Ensembl
chr2:144388872..144389054hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254490
Samples
Known GenesARHGAP15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549172
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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