A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047862



Internal ID20614902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39197689..39199546hg38UCSC Ensembl
chr19:39688329..39690186hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381858
hg191858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530587
Supporting Variants
Samples
Known GenesNCCRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0011


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