A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15762596



Internal ID22097097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169761277..169761583hg38UCSC Ensembl
chr1:169730418..169730724hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4440331
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15762596
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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