A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15767828



Internal ID22102299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15791223..15791626hg38UCSC Ensembl
chr4:15792846..15793249hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4447772
Supporting Variants
Samples
Known GenesCD38
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15767828
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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