A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229155



Internal ID20796195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51756534..51757145hg38UCSC Ensembl
chr10:53516294..53516905hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580272
Supporting Variants
Samples
Known GenesPRKG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229155
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00026


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