A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575549



Internal ID20948620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73839193..73995312hg38UCSC Ensembl
chr4:74704910..74861029hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38156120
hg19156120
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5334n223
Supporting Variantsnssv18266026
Samples
Known GenesCXCL1, PF4, PF4V1, PPBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575549
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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