A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045975



Internal ID19135194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98568588..98592611hg38UCSC Ensembl
Innerchr14:99034925..99058948hg19UCSC Ensembl
Innerchr14:98104678..98128701hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3824024
hg1924024
hg1824024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1967n100
Supporting Variantsnssv3532703
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)nsv1045975
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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