A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390439



Internal ID21047992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:61809735..61810519hg38UCSC Ensembl
chr4:62675453..62676237hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118478
Samples
Known GenesLPHN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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