A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702624



Internal ID126290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84165874..84238500hg38UCSC Ensembl
chr15:84834626..84907252hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3872627
hg1972627
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144402
Supporting Variants
Samples
Known GenesGOLGA6L4, LOC100505679, LOC388152, LOC440300, LOC642423
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702624
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.043253


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