A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375907



Internal ID22601576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96118966..96119017hg38UCSC Ensembl
chr15:96662195..96662246hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938649
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375907
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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