A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037675



Internal ID19126894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22162256..22478914hg38UCSC Ensembl
Innerchr14:22630152..22947903hg19UCSC Ensembl
Innerchr14:21699992..22017743hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38316659
hg19317752
hg18317752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1805n100
Supporting Variantsnssv3532225
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)nsv1037675
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer