A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253057



Internal ID20820097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39119045..39119970hg38UCSC Ensembl
chr1:39584717..39585642hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38926
hg19926
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551958
Supporting Variants
Samples
Known GenesMACF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253057
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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