A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252585



Internal ID20819625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49841187..49842037hg38UCSC Ensembl
chr20:48457724..48458574hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38851
hg19851
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597225
Supporting Variants
Samples
Known GenesSLC9A8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252585
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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