A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039115



Internal ID19128334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48319210..48442110hg38UCSC Ensembl
Innerchr14:48788413..48911313hg19UCSC Ensembl
Innerchr14:47858163..47981063hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38122901
hg19122901
hg18122901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1918n100
Supporting Variantsnssv3531002
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)nsv1039115
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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