A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249661



Internal ID20816701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51555209..51555667hg38UCSC Ensembl
chr1:52020881..52021339hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549610
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249661
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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