A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251236



Internal ID20818276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6543217..6544088hg38UCSC Ensembl
chr1:6603277..6604148hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38872
hg19872
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540214
Supporting Variants
Samples
Known GenesNOL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251236
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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