A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17378370



Internal ID22436240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4955807..4955883hg38UCSC Ensembl
chr17:4859102..4859178hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938169
Supporting Variants
Samples
Known GenesENO3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17378370
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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