A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538214



Internal ID20911537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24331265..24332118hg38UCSC Ensembl
chr2:24554134..24554987hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38854
hg19854
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258111
Samples
Known GenesITSN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538214
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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