A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584256



Internal ID21532792
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 Variantsnssv17134142
SamplesNA19239
Known GenesC4orf19
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584256
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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