A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17130488



Internal ID21505325
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 StatusS
Merged Variantsnsv5572712
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17130488
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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