A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529136



Internal ID22398529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78679356..78679427hg38UCSC Ensembl
chr17:76675438..76675509hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282487, nssv14282488
SamplesHG00731, HG00733
Known GenesCYTH1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529136
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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