A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025150



Internal ID21934493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90630742..90631075hg38UCSC Ensembl
chr15:91173974..91174307hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606622
Samples
Known GenesCRTC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025150
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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