A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441011



Internal ID22107190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16131445..16133677hg38UCSC Ensembl
chr2:16271567..16273799hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg382233
hg192233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760379
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441011
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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