A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389435



Internal ID22447305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81805610..81805706hg38UCSC Ensembl
chr17:79763486..79763582hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929303
Supporting Variants
Samples
Known GenesGCGR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389435
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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