A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440990



Internal ID22107168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57190356..57190428hg38UCSC Ensembl
chr20:55765412..55765484hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763692
Samples
Known GenesBMP7
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440990
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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