A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908952



Internal ID22684162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29629592..29630061hg38UCSC Ensembl
chr10:29918521..29918990hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362441
Samples
Known GenesSVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908952
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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