A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542756



Internal ID20869200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:172149066..172149528hg38UCSC Ensembl
chr2:173013794..173014256hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256100
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542756
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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