A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043036



Internal ID19132255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27330727..27374103hg38UCSC Ensembl
Innerchr14:27799933..27843309hg19UCSC Ensembl
Innerchr14:26869773..26913149hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3843377
hg1943377
hg1843377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528565, nssv3528564
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)nsv1043036
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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