A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439998



Internal ID22106175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138739198..138739275hg38UCSC Ensembl
chr4:139660352..139660429hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15755919
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439998
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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