A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098992



Internal ID21483742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40529727..40531387hg38UCSC Ensembl
chr15:40821926..40823586hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381661
hg191661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590125
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098992
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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