A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5543699



Internal ID317927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36363390..36363390hg38UCSC Ensembl
chr6:36331167..36331167hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16981327
Samples
Known GenesETV7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5543699
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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