A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438874



Internal ID22105051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58552116..58552372hg38UCSC Ensembl
chr1:59017788..59018044hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761028
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438874
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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