A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556994



Internal ID20930065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78365214..78366206hg38UCSC Ensembl
chr5:77661038..77662030hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38993
hg19993
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270271
Samples
Known GenesSCAMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556994
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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