A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079744



Internal ID21454755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42350281..42350806hg38UCSC Ensembl
chr15:42642479..42643004hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585389
Supporting Variants
SamplesHG02011
Known GenesGANC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079744
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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