A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407649



Internal ID21065202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:84262491..84312605hg38UCSC Ensembl
chr5:83558309..83608423hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3850115
hg1950115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135247
Samples
Known GenesEDIL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407649
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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