A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882802



Internal ID22657779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110488373..110489605hg38UCSC Ensembl
chr1:111030995..111032227hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381233
hg191233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358139
Samples
Known GenesCYMP, LOC440602
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882802
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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