A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539899



Internal ID20913194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27465954..27472252hg38UCSC Ensembl
chr3:27507445..27513743hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg386299
hg196299
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262643
Samples
Known GenesSLC4A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539899
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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