A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391713



Internal ID22449583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45669951..45670034hg38UCSC Ensembl
chr19:46173209..46173292hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947056
Supporting Variants
Samples
Known GenesGIPR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17391713
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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