A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437906



Internal ID22104086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11885356..11885473hg38UCSC Ensembl
chr10:11927355..11927472hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765681
Samples
Known GenesPROSER2-AS1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437906
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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