A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355484



Internal ID22235151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86277977..86278047hg38UCSC Ensembl
chr10:88037734..88037804hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527611
Supporting Variants
SamplesHG00733
Known GenesGRID1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355484
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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