A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572712



Internal ID21521104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37037126..37037199hg38UCSC Ensembl
chr4:37038748..37038821hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130488
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572712
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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