A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443782



Internal ID22109963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177451316..177451532hg38UCSC Ensembl
chr5:176878317..176878533hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15768319
Samples
Known GenesPRR7
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443782
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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