A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747464



Internal ID21390260
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 StatusS
Merged Variantsnsv4434794
Supporting Variants
SamplesNB11
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747464
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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