A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053264



Internal ID19142483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:91781715..91827174hg38UCSC Ensembl
Innerchr14:92248059..92293518hg19UCSC Ensembl
Innerchr14:91317812..91363271hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3845460
hg1945460
hg1845460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532583
Samples
Known GenesTC2N
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053264
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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