A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250195



Internal ID20817235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24376047..24377007hg38UCSC Ensembl
chr1:24702537..24703497hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38961
hg19961
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554429
Supporting Variants
Samples
Known GenesSTPG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250195
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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