A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565561



Internal ID20938632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:129568257..129612028hg38UCSC Ensembl
chr4:130489412..130533183hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3843772
hg1943772
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565561
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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