A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407997



Internal ID22465867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14488709..14490910hg38UCSC Ensembl
chr19:14599521..14601722hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382202
hg192202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933955
Supporting Variants
Samples
Known GenesGIPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407997
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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