A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249538



Internal ID20816578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:185182927..185183462hg38UCSC Ensembl
chr1:185152059..185152594hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544696
Supporting Variants
Samples
Known GenesSWT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249538
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00077


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