A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853753



Internal ID22628688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28936368..28937567hg38UCSC Ensembl
chr15:29228571..29229770hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471069
Samples
Known GenesAPBA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853753
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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