A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045557



Internal ID19134776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38575040..38633019hg38UCSC Ensembl
Innerchr14:39044244..39102223hg19UCSC Ensembl
Innerchr14:38113995..38171974hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3857980
hg1957980
hg1857980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1874n100
Supporting Variantsnssv3528649
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)nsv1045557
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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