A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043014



Internal ID19132233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:45356841..45555776hg38UCSC Ensembl
Innerchr14:45826044..46024979hg19UCSC Ensembl
Innerchr14:44895794..45094729hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38198936
hg19198936
hg18198936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1905n100
Supporting Variantsnssv3531633, nssv3531632
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)nsv1043014
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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