A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527081



Internal ID22396465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87408464..87408588hg38UCSC Ensembl
chr6:88118182..88118306hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8002n152
Supporting Variantsnssv14329543, nssv14329547, nssv14329544, nssv14329546, nssv14329545
SamplesNA19239, HG00731, HG00732, NA19240, HG00733
Known GenesC6orf165
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527081
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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