A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15753561



Internal ID21388991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157278889..157283338hg38UCSC Ensembl
chr6:157699921..157704370hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384450
hg194450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434796
Supporting Variants
SamplesNB08
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15753561
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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