A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042759



Internal ID19131978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83174383..83240252hg38UCSC Ensembl
Innerchr14:83640727..83706596hg19UCSC Ensembl
Innerchr14:82710480..82776349hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3865870
hg1965870
hg1865870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1945n100
Supporting Variantsnssv3532340
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)nsv1042759
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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