A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371652



Internal ID22597321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41311822..41312231hg38UCSC Ensembl
chr15:41604020..41604429hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931273
Supporting Variants
Samples
Known GenesOIP5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371652
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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