A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335212



Internal ID22195910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25896164..25896232hg38UCSC Ensembl
chr10:26185093..26185161hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529662
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335212
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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