A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409599



Internal ID22467469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2820736..2821733hg38UCSC Ensembl
chr19:2820734..2821731hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38998
hg19998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936180
Supporting Variants
Samples
Known GenesZNF554
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409599
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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