A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590075



Internal ID21538643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88521745..88521796hg38UCSC Ensembl
chr16:88588153..88588204hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099139
SamplesHG03486
Known GenesZFPM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590075
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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