A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542936



Internal ID20916187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101552684..101553283hg38UCSC Ensembl
chr2:102169146..102169745hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255738
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542936
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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