A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536062



Internal ID20909415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:152144680..152146042hg38UCSC Ensembl
chr2:153001194..153002556hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg381363
hg191363
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4155n223
Supporting Variantsnssv18254601
Samples
Known GenesSTAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536062
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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