A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437903



Internal ID22104083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10767840..10768010hg38UCSC Ensembl
chr10:10809803..10809973hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764616
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437903
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