A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053265



Internal ID19142484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:82469794..82516716hg38UCSC Ensembl
Innerchr14:82936138..82983060hg19UCSC Ensembl
Innerchr14:82005891..82052813hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3846923
hg1946923
hg1846923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713534
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)nsv1053265
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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