A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049661



Internal ID19138880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48319210..48444284hg38UCSC Ensembl
Innerchr14:48788413..48913487hg19UCSC Ensembl
Innerchr14:47858163..47983237hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38125075
hg19125075
hg18125075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1918n100
Supporting Variantsnssv3713489, nssv3531003
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)nsv1049661
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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