A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041829



Internal ID19131048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47762752..47817385hg38UCSC Ensembl
Innerchr14:48231955..48286588hg19UCSC Ensembl
Innerchr14:47301705..47356338hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3854634
hg1954634
hg1854634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1914n100
Supporting Variantsnssv3530978, nssv3530979
Samples
Known GenesLINC00648
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041829
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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