A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953269



Internal ID21373338
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 Variantsnssv15176086
SamplesHG002
Known GenesCYTH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953269
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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