A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527300



Internal ID22396686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76310157..76310330hg38UCSC Ensembl
chr17:74306238..74306411hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281810, nssv14281811
SamplesNA19238, NA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527300
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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