A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433782



Internal ID21395784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38717701..38719928hg38UCSC Ensembl
chr2:38944843..38947070hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg382228
hg192228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv408n172
Supporting Variantsnssv15750483, nssv15750994
SamplesSMI034, MDQ010
Known GenesGALM
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433782
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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