A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910377



Internal ID22685588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91055626..91055946hg38UCSC Ensembl
chr10:92815383..92815703hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359183
Samples
Known GenesLINC00502
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910377
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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