A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126581



Internal ID21414359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37003181..37003493hg38UCSC Ensembl
chr4:37004803..37005115hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571371
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126581
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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