A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706388



Internal ID21378664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8449527..8449833hg38UCSC Ensembl
chr19:8514411..8514717hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392277
Supporting Variants
Samples
Known GenesHNRNPM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706388
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.962644


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