A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572714



Internal ID21521106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77183913..77184068hg38UCSC Ensembl
chr4:78105066..78105221hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128278
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572714
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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