A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091294



Internal ID21482076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88461137..88461137hg38UCSC Ensembl
chr16:88527545..88527545hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654437
Supporting Variants
SamplesHG03683
Known GenesZFPM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091294
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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