A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394678



Internal ID22452548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7473682..7475104hg38UCSC Ensembl
chr19:7538568..7539990hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381423
hg191423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932336
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394678
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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