A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905306



Internal ID22680491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16124701..16125376hg38UCSC Ensembl
chr5:16124810..16125485hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38676
hg19676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419664
Samples
Known GenesMARCH11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905306
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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