A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564027



Internal ID18862308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1907315..1980374hg38UCSC Ensembl
Innerchr18:1907316..1980375hg19UCSC Ensembl
Innerchr18:1897316..1970375hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3873060
hg1973060
hg1873060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059831
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564027
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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