A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396287



Internal ID21053840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107457374..107457820hg38UCSC Ensembl
chr5:106793075..106793521hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124225
Samples
Known GenesEFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396287
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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