A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545495



Internal ID20918725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37387382..37825847hg38UCSC Ensembl
chr2:37614525..38052990hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38438466
hg19438466
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260187
Samples
Known GenesCDC42EP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545495
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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