A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17557553



Internal ID21881908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38996461..38996561hg38UCSC Ensembl
chr8:38853980..38854080hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018903
Supporting Variants
Samples
Known GenesTM2D2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17557553
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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