A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248935



Internal ID20815975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203651776..203652446hg38UCSC Ensembl
chr1:203620904..203621574hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549848
Supporting Variants
Samples
Known GenesATP2B4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248935
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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