A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17002344



Internal ID69172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114639290..114639341hg38UCSC Ensembl
chr7:114279345..114279396hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5401877
Supporting Variants
Samples
Known GenesFOXP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17002344
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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