A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039658



Internal ID19128877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28096481..28140455hg38UCSC Ensembl
Innerchr14:28565687..28609661hg19UCSC Ensembl
Innerchr14:27635438..27679412hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3843975
hg1943975
hg1843975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1862n100
Supporting Variantsnssv3528577
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)nsv1039658
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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