A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355135



Internal ID22209627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121509809..121515009hg38UCSC Ensembl
chr10:123269323..123274523hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg385201
hg195201
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229341
Supporting Variants
SamplesHG00732
Known GenesFGFR2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355135
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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