A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527517



Internal ID22396904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137311761..137311992hg38UCSC Ensembl
chr7:136996508..136996739hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14339098, nssv14339096, nssv14339097
SamplesNA19238, NA19239, NA19240
Known GenesPTN
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527517
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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