A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257645



Internal ID20824685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60564..381949hg38UCSC Ensembl
chr2:60564..381949hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38321386
hg19321386
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555528
Supporting Variants
Samples
Known GenesACP1, FAM150B, SH3YL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257645
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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