A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531019



Internal ID18482614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:50676760..50853094hg38UCSC Ensembl
Innerchr14:51143478..51319812hg19UCSC Ensembl
Innerchr14:50213228..50389562hg18UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38176335
hg19176335
hg18176335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040775
Supporting Variants
Samples
Known GenesNIN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531019
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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