A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253934



Internal ID20820974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85254368..85255325hg38UCSC Ensembl
chr1:85720051..85721008hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38958
hg19958
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537915
Supporting Variants
Samples
Known GenesC1orf52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253934
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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