A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527538



Internal ID22396925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35842225..35842338hg38UCSC Ensembl
chr6:35810002..35810115hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14325570, nssv14325571
SamplesHG00732, HG00733
Known GenesSRPK1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527538
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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