A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17440807



Internal ID22498677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4733640..4736037hg38UCSC Ensembl
chr6:4733874..4736271hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg382398
hg192398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896225
Supporting Variants
Samples
Known GenesCDYL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17440807
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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