A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944294



Internal ID21364363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13782608..13782706hg38UCSC Ensembl
chr17:13685925..13686023hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15175994
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944294
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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