A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042444



Internal ID19131663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:45356841..45554732hg38UCSC Ensembl
Innerchr14:45826044..46023935hg19UCSC Ensembl
Innerchr14:44895794..45093685hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38197892
hg19197892
hg18197892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1905n100
Supporting Variantsnssv3531630, nssv3531631
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)nsv1042444
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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