A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646800



Internal ID21838847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34753398..34753452hg38UCSC Ensembl
chr21:36125695..36125749hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042496
Supporting Variants
Samples
Known GenesLOC100506385
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646800
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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