A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434897



Internal ID21396899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:257001..383000hg38UCSC Ensembl
chr6:257001..383000hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38126000
hg19126000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv671n172
Supporting Variantsnssv15746481, nssv15745655, nssv15749177
SamplesBTQ038, BTQ055, SMI018
Known GenesDUSP22
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434897
Frequency
Sample Size15
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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