A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389088



Internal ID22446958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72700665..72704103hg38UCSC Ensembl
chr15:72993006..72996444hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg383439
hg193439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931153
Supporting Variants
Samples
Known GenesBBS4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389088
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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