A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027209



Internal ID20594249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83899873..83900260hg38UCSC Ensembl
chr15:84568625..84569012hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502134
Supporting Variants
Samples
Known GenesADAMTSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027209
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0007


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