A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573253



Internal ID20946324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56493359..56493997hg38UCSC Ensembl
chr4:57359525..57360163hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265803
Samples
Known GenesSRP72
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573253
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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