A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380090



Internal ID22437960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27767600..27767689hg38UCSC Ensembl
chr15:28012746..28012835hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936879
Supporting Variants
Samples
Known GenesOCA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380090
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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