A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394692



Internal ID22452562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7374419..7375013hg38UCSC Ensembl
chr19:7439305..7439899hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939160
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394692
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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