A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527692



Internal ID22397079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38144172..38144223hg38UCSC Ensembl
chr6:38111948..38111999hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7861n152
Supporting Variantsnssv14325666, nssv14325665, nssv14325667
SamplesNA19239, NA19240, HG00514
Known GenesZFAND3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527692
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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