A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021849



Internal ID21931192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90080550..90081728hg38UCSC Ensembl
chr15:90623782..90624960hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381179
hg191179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610044
Samples
Known GenesZNF710
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021849
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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