A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252672



Internal ID20819712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9216153..9216744hg38UCSC Ensembl
chr1:9276212..9276803hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548243
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252672
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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