A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376481



Internal ID21034034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37098081..37098639hg38UCSC Ensembl
chr4:37099703..37100261hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115932
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376481
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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