A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570612



Internal ID20943683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:128077501..128078413hg38UCSC Ensembl
chr5:127413193..127414105hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg38913
hg19913
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267278
Samples
Known GenesFLJ33630
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570612
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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