A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647202



Internal ID21839249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34993689..34993785hg38UCSC Ensembl
chr21:36365986..36366082hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046083
Supporting Variants
Samples
Known GenesRUNX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647202
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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