A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433123



Internal ID21395125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36958252..36959924hg38UCSC Ensembl
chr1:37423853..37425525hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381673
hg191673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv14n172
Supporting Variantsnssv15747747
SamplesBTQ055
Known GenesGRIK3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433123
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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