A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908696



Internal ID22683906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5480009..5480096hg38UCSC Ensembl
chr10:5521972..5522059hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357470
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908696
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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