A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376625



Internal ID21034178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62770611..62771065hg38UCSC Ensembl
chr4:63636329..63636783hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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