A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550063



Internal ID20923215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100154243..100154686hg38UCSC Ensembl
chr3:99873087..99873530hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258858
Samples
Known GenesCMSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550063
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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