A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902624



Internal ID22677784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102844872..102954508hg38UCSC Ensembl
chr5:102180576..102290212hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38109637
hg19109637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428245
Samples
Known GenesPAM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902624
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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