A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250459



Internal ID20817499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61138563..61139185hg38UCSC Ensembl
chr1:61604235..61604857hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38623
hg19623
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552540
Supporting Variants
Samples
Known GenesNFIA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250459
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00022


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