A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525277



Internal ID301443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95460460..95460551hg38UCSC Ensembl
chr15:96003689..96003780hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703332
Samples
Known GenesLINC00924
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525277
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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