A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439866



Internal ID22106043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44969686..44970828hg38UCSC Ensembl
chr19:45472943..45474085hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381143
hg191143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759530
Samples
Known GenesCLPTM1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439866
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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