A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3952778



Internal ID21372847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:46099028..46099351hg38UCSC Ensembl
chr17:44176394..44176717hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15176038
SamplesHG002
Known GenesKANSL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3952778
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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