A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388923



Internal ID22446793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95301994..96435598hg38UCSC Ensembl
chr15:95845223..96978828hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381133605
hg191133606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938972
Supporting Variants
Samples
Known GenesLINC00924, LOC400456, MIR1469, NR2F2, NR2F2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388923
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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