A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433253



Internal ID21395255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23122557..23122995hg38UCSC Ensembl
chr20:23103194..23103632hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv454n172
Supporting Variantsnssv15747204, nssv15754268, nssv15747776, nssv15754153
SamplesNB08, BTQ038, NB10, MDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433253
Frequency
Sample Size15
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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