A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377484



Internal ID21035037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119494159..119494612hg38UCSC Ensembl
chr4:120415314..120415767hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38454
hg19454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107202
Samples
Known GenesLOC645513, PDE5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377484
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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