A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574056



Internal ID20947127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34994911..34996819hg38UCSC Ensembl
chr5:34995016..34996924hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg381909
hg191909
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574056
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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