A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580855



Internal ID20953926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55904015..55904404hg38UCSC Ensembl
chr15:56196213..56196602hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241095
Samples
Known GenesNEDD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580855
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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