A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564148



Internal ID18862429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:29134182..29155685hg38UCSC Ensembl
Innerchr18:26714146..26735650hg19UCSC Ensembl
Innerchr18:24968144..24989648hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3821504
hg1921505
hg1821505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065998
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)nssv3564148
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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