A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938544



Internal ID22713925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97532799..97599526hg38UCSC Ensembl
chr15:98076029..98142756hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3866728
hg1966728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938544
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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