A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257656



Internal ID20824696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60718295..60718900hg38UCSC Ensembl
chr2:60945430..60946035hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539208
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257656
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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