A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538590



Internal ID20911903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:44828150..44828721hg38UCSC Ensembl
chr2:45055289..45055860hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258004
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538590
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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