A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568486



Internal ID21760529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102256229..102256229hg38UCSC Ensembl
chr7:101899509..101899509hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076793
Supporting Variants
Samples
Known GenesCUX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568486
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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