A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559761



Internal ID20932832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128008061..128008291hg38UCSC Ensembl
chr4:128929216..128929446hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263735
Samples
Known GenesC4orf29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559761
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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