A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15762938



Internal ID22097428
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 StatusS
Merged Variantsnsv4437615
Supporting Variants
Samples
Known GenesENTPD8
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15762938
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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