A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564104



Internal ID18515699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11892846..11911144hg38UCSC Ensembl
Innerchr18:11892845..11911143hg19UCSC Ensembl
Innerchr18:11882845..11901143hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3818299
hg1918299
hg1818299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059775
Supporting Variants
Samples
Known GenesMPPE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564104
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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