A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436930



Internal ID215535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16866723..16876833hg38UCSC Ensembl
chr4:16868346..16878456hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3810111
hg1910111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735053
Samples
Known GenesLDB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436930
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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