A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407980



Internal ID21065533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160195899..160197054hg38UCSC Ensembl
chr5:159622906..159624061hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg381156
hg191156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127492
Samples
Known GenesFABP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407980
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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