A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531229



Internal ID18829510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:81721797..82197253hg38UCSC Ensembl
Innerchr14:82188141..82663597hg19UCSC Ensembl
Innerchr14:81257894..81733350hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38475457
hg19475457
hg18475457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042626
Supporting Variants
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)nssv3531229
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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