A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569616



Internal ID20942687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2544444..2545148hg38UCSC Ensembl
chr4:2546171..2546875hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569616
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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