A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400108



Internal ID21057661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95672125..95672719hg38UCSC Ensembl
chr5:95007829..95008423hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135614
Samples
Known GenesSPATA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400108
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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