A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569915



Internal ID20942986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2011193..2011767hg38UCSC Ensembl
chr4:2012920..2013494hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569915
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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