A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252364



Internal ID20819404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29081805..29082417hg38UCSC Ensembl
chr1:29408317..29408929hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551527
Supporting Variants
Samples
Known GenesEPB41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252364
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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