A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001172



Internal ID21910515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38457812..38458370hg38UCSC Ensembl
chr8:38315330..38315888hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564144
Samples
Known GenesFGFR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001172
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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