A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251063



Internal ID20818103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37093415..37094367hg38UCSC Ensembl
chr1:37559016..37559968hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38953
hg19953
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548182
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251063
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0001


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