A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536812



Internal ID21861167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6228417..6228617hg38UCSC Ensembl
chr1:6288477..6288677hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984649
Supporting Variants
Samples
Known GenesICMT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536812
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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