A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434794



Internal ID21396796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157278889..157282357hg38UCSC Ensembl
chr6:157699921..157703389hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383469
hg193469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv722n172
Supporting Variantsnssv15747464
SamplesNB11
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434794
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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