A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388082



Internal ID22445952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17805298..17805349hg38UCSC Ensembl
chr17:17708612..17708663hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928366
Supporting Variants
Samples
Known GenesRAI1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388082
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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