A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541027



Internal ID20914312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26004959..26005938hg38UCSC Ensembl
chr2:26227828..26228807hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38980
hg19980
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541027
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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