A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5544706



Internal ID318824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38184864..38184904hg38UCSC Ensembl
chr7:38224466..38224506hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16996210
Samples
Known GenesSTARD3NL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5544706
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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