A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712283



Internal ID19010564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:37380537..37459548hg38UCSC Ensembl
Innerchr14:37849742..37928753hg19UCSC Ensembl
Innerchr14:36919493..36998504hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3879012
hg1979012
hg1879012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043093
Supporting Variants
Samples
Known GenesMIPOL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712283
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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