A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544272



Internal ID20917511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27648717..27648985hg38UCSC Ensembl
chr2:27871584..27871852hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3816n223
Supporting Variantsnssv18257556
Samples
Known GenesGPN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544272
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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