A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541606



Internal ID20914888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175920478..175920927hg38UCSC Ensembl
chr2:176785206..176785655hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541606
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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