A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712275



Internal ID19010556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27886637..27956088hg38UCSC Ensembl
Innerchr14:28355843..28425294hg19UCSC Ensembl
Innerchr14:27425683..27495134hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3869452
hg1969452
hg1869452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052542
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)nssv3712275
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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