A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039578



Internal ID21948921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88461029..88461110hg38UCSC Ensembl
chr16:88527437..88527518hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635233
Samples
Known GenesZFPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039578
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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