A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747921



Internal ID20523943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44272227..44272304hg38UCSC Ensembl
chr19:44776380..44776457hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290759
Samples
Known GenesZNF233
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747921
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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