A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042896



Internal ID19132115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48952406..49018981hg38UCSC Ensembl
Innerchr14:49421609..49488184hg19UCSC Ensembl
Innerchr14:48491359..48557934hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3866576
hg1966576
hg1866576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531013
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)nsv1042896
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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