A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937627



Internal ID22712998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83769696..83771131hg38UCSC Ensembl
chr15:84438448..84439883hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381436
hg191436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371178
Samples
Known GenesADAMTSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937627
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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