A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129614



Internal ID21497944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1828362..1828627hg38UCSC Ensembl
chr4:1830089..1830354hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567138
Supporting Variants
SamplesNA19238
Known GenesLETM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129614
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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