A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903044



Internal ID22678208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:44710026..44763207hg38UCSC Ensembl
chr5:44710128..44763309hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3853182
hg1953182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903044
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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