A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395513



Internal ID22453383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57195540..57202954hg38UCSC Ensembl
chr19:57706908..57714322hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg387415
hg197415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928120
Supporting Variants
Samples
Known GenesZNF264
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395513
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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