A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404826



Internal ID22462696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:26205932..26285099hg38UCSC Ensembl
chr20:26186568..26265735hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3879168
hg1979168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5948418
Supporting Variants
Samples
Known GenesLOC284801, MIR663A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404826
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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