A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432954



Internal ID21394956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150631108..150632171hg38UCSC Ensembl
chr1:150603584..150604647hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381064
hg191064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15751670
SamplesMDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432954
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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