A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569676



Internal ID20942747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95833829..96527291hg38UCSC Ensembl
chr5:95169533..95862995hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38693463
hg19693463
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267745
Samples
Known GenesC5orf27, ELL2, MIR583, PCSK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569676
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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