A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543502



Internal ID20870355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27986224..27986512hg38UCSC Ensembl
chr1:28312735..28313023hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249060
Samples
Known GenesEYA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543502
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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