A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906536



Internal ID22681737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37460968..37462157hg38UCSC Ensembl
chr4:37462590..37463779hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381190
hg191190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428769
Samples
Known GenesC4orf19
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906536
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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