A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583283



Internal ID21531806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163580788..163581100hg38UCSC Ensembl
chr4:164501940..164502252hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136632
SamplesHG00731
Known GenesMARCH1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583283
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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