A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924443



Internal ID22699670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:85577978..85594307hg38UCSC Ensembl
chr10:87337735..87354064hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3816330
hg1916330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353722
Samples
Known GenesGRID1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924443
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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