A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437663



Internal ID22103843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1046461..1047339hg38UCSC Ensembl
chr10:1092401..1093279hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38879
hg19879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15755953
Samples
Known GenesIDI1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437663
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