A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17429509



Internal ID22487379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:66358948..66359056hg38UCSC Ensembl
chr4:67224666..67224774hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5899718
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17429509
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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