A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070305



Internal ID21487390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45625577..45625577hg38UCSC Ensembl
chr10:46121025..46121025hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637174
Supporting Variants
SamplesNA18534
Known GenesZFAND4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070305
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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