A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908363



Internal ID22683573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101819584..101819653hg38UCSC Ensembl
chr10:103579341..103579410hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361222
Samples
Known GenesKCNIP2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908363
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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