A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371281



Internal ID22596950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36569591..36569670hg38UCSC Ensembl
chr15:36861792..36861871hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371281
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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