A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250477



Internal ID20817517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61712572..61719589hg38UCSC Ensembl
chr1:62178244..62185261hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg387018
hg197018
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549715
Supporting Variants
Samples
Known GenesTM2D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250477
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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