A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169848



Internal ID21313659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:38382143..38383652hg38UCSC Ensembl
Outerchr20:38376710..38390010hg38UCSC Ensembl
Innerchr20:37010785..37012294hg19UCSC Ensembl
Outerchr20:37005352..37018652hg19UCSC Ensembl
Innerchr20:36444199..36445708hg18UCSC Ensembl
Outerchr20:36438766..36452066hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3813301
hg1913301
hg1813301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245249
SamplesSNI_3
Known GenesLBP
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169848
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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