A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527611



Internal ID22396998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86277977..86278047hg38UCSC Ensembl
chr10:88037734..88037804hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355484, nssv14355483
SamplesHG00732, HG00733
Known GenesGRID1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527611
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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