A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250409



Internal ID20817449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35510752..35512180hg38UCSC Ensembl
chr1:35976353..35977781hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381429
hg191429
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550069
Supporting Variants
Samples
Known GenesKIAA0319L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250409
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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