A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571855



Internal ID20944926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157124035..157124449hg38UCSC Ensembl
chr5:156551046..156551460hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269415
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571855
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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