A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738823



Internal ID20514794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88032841..88032988hg38UCSC Ensembl
chr5:87328658..87328805hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277570
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738823
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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