A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528722



Internal ID22398112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4031226..4031302hg38UCSC Ensembl
chr10:4073418..4073494hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv757n152
Supporting Variantsnssv14326472, nssv14326470, nssv14326471
SamplesHG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528722
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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