A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545991



Internal ID20919211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219134921..219136491hg38UCSC Ensembl
chr2:219999643..220001213hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381571
hg191571
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4288n223
Supporting Variantsnssv18259366
Samples
Known GenesNHEJ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545991
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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