A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227701



Internal ID22370113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87775421..87775533hg38UCSC Ensembl
chr10:89535178..89535290hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355534, nssv14355532, nssv14355533
SamplesHG00512, HG00513, HG00514
Known GenesATAD1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227701
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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