A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252524



Internal ID21309631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:66866438..66900738hg38UCSC Ensembl
Outerchr18:66863456..66907043hg38UCSC Ensembl
Innerchr18:64533675..64567975hg19UCSC Ensembl
Outerchr18:64530693..64574280hg19UCSC Ensembl
Innerchr18:62684655..62718955hg18UCSC Ensembl
Outerchr18:62681673..62725260hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3843588
hg1943588
hg1843588
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169561
Supporting Variants
SamplesNGO_51
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14252524
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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