A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540312



Internal ID20913602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:136086934..136087067hg38UCSC Ensembl
chr2:136844504..136844637hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540312
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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