A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044764



Internal ID19133983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44712945..44758717hg38UCSC Ensembl
Innerchr14:45182148..45227920hg19UCSC Ensembl
Innerchr14:44251898..44297670hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3845773
hg1945773
hg1845773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1903n100
Supporting Variantsnssv3530429, nssv3530427, nssv3530426, nssv3530431, nssv3530430, nssv3713465, nssv3530428
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)nsv1044764
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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