A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567663



Internal ID20940734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:80266608..80271233hg38UCSC Ensembl
chr4:81187762..81192387hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg384626
hg194626
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265340
Samples
Known GenesFGF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567663
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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