A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539922



Internal ID20913217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28939697..28940482hg38UCSC Ensembl
chr2:29162563..29163348hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg38786
hg19786
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3817n223
Supporting Variantsnssv18257592
Samples
Known GenesWDR43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539922
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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