A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052760



Internal ID19141979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44713431..44754498hg38UCSC Ensembl
Innerchr14:45182634..45223701hg19UCSC Ensembl
Innerchr14:44252384..44293451hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3841068
hg1941068
hg1841068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1903n100
Supporting Variantsnssv3530435, nssv3530434
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)nsv1052760
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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