A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542846



Internal ID20916097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32253973..32254625hg38UCSC Ensembl
chr2:32479042..32479694hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38653
hg19653
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260072
Samples
Known GenesNLRC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542846
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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