A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098021



Internal ID21507241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41949051..41949051hg38UCSC Ensembl
chr15:42241249..42241249hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662331
Supporting Variants
SamplesNA19983
Known GenesEHD4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098021
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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