A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562250



Internal ID20935321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55360452..55360943hg38UCSC Ensembl
chr4:56226619..56227110hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266422
Samples
Known GenesSRD5A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562250
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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