A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036267



Internal ID19125486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46022625..46335531hg38UCSC Ensembl
Innerchr14:46491828..46804734hg19UCSC Ensembl
Innerchr14:45561578..45874484hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38312907
hg19312907
hg18312907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531654
Samples
Known GenesLINC00871
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036267
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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