A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17581443



Internal ID21773486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73377583..73377583hg38UCSC Ensembl
chr10:75137341..75137341hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6082057
Supporting Variants
Samples
Known GenesANXA7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17581443
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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