A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443448



Internal ID22109631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150084360..150084467hg38UCSC Ensembl
chr5:149463923..149464030hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762189
Samples
Known GenesCSF1R
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443448
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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