A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369913



Internal ID22595582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73993779..73993906hg38UCSC Ensembl
chr15:74286120..74286247hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933251
Supporting Variants
Samples
Known GenesSTOML1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369913
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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