A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355933



Internal ID22264941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126051571..126051631hg38UCSC Ensembl
chr10:127740140..127740200hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3219244
Supporting Variants
SamplesNA19238
Known GenesADAM12
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355933
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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