A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050803



Internal ID19140022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48315557..48444284hg38UCSC Ensembl
Innerchr14:48784760..48913487hg19UCSC Ensembl
Innerchr14:47854510..47983237hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38128728
hg19128728
hg18128728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1918n100
Supporting Variantsnssv3530996
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)nsv1050803
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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