A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038162



Internal ID19127381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38481411..38564740hg38UCSC Ensembl
Innerchr14:38950615..39033944hg19UCSC Ensembl
Innerchr14:38020366..38103695hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3883330
hg1983330
hg1883330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1873n100
Supporting Variantsnssv3712284
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)nsv1038162
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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