A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238904



Internal ID20805944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65575314..65575833hg38UCSC Ensembl
chr15:65867652..65868171hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586412
Supporting Variants
Samples
Known GenesPTPLAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238904
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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