A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434895



Internal ID21396897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24878885..24879196hg38UCSC Ensembl
chr6:24879113..24879424hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750595, nssv15750058
SamplesSMI034, SMI041
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434895
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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