A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380129



Internal ID21037682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62058295..62059087hg38UCSC Ensembl
chr4:62924013..62924805hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38793
hg19793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118503
Samples
Known GenesLPHN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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