A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566705



Internal ID21515033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145700107..145700190hg38UCSC Ensembl
chr4:146621259..146621342hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125568
SamplesNA19239
Known GenesC4orf51
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566705
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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