A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443449



Internal ID22109632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150366628..150366954hg38UCSC Ensembl
chr5:149746191..149746517hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758079
Samples
Known GenesTCOF1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443449
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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