A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437615



Internal ID22103795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137440688..137440853hg38UCSC Ensembl
chr9:140335140..140335305hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762938
Samples
Known GenesENTPD8
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437615
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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