A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041881



Internal ID19131100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44583103..44660211hg38UCSC Ensembl
Innerchr14:45052306..45129414hg19UCSC Ensembl
Innerchr14:44122056..44199164hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3877109
hg1977109
hg1877109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530328
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)nsv1041881
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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