A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4449512



Internal ID22115689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32974272..32974399hg38UCSC Ensembl
chr1:33439873..33440000hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761014
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4449512
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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