A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543789



Internal ID21868144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69964323..69964736hg38UCSC Ensembl
chr3:70013474..70013887hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5994436
Supporting Variants
Samples
Known GenesMITF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543789
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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