A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548674



Internal ID20921858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94893497..94894095hg38UCSC Ensembl
chr1:95359053..95359651hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38599
hg19599
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253952
Samples
Known GenesSLC44A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548674
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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