A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037101



Internal ID19126320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40049637..40137182hg38UCSC Ensembl
Innerchr14:40518841..40606386hg19UCSC Ensembl
Innerchr14:39588592..39676137hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3887546
hg1987546
hg1887546
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1877n100
Supporting Variantsnssv3712292, nssv3530137
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)nsv1037101
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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