A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927563



Internal ID22702791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92972557..92972869hg38UCSC Ensembl
chr15:93515787..93516099hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377804
Samples
Known GenesCHD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927563
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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