A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3478434



Internal ID18721400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26377839..26420321hg38UCSC Ensembl
Innerchr1:26704330..26746812hg19UCSC Ensembl
Innerchr1:26576917..26619399hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3842483
hg1942483
hg1842483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014791
Supporting Variants
Samples
Known GenesLIN28A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3478434
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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