A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761681



Internal ID22096155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:65670024..65670355hg38UCSC Ensembl
chr1:66135707..66136038hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4438630
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761681
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer