A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3491827



Internal ID19079468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:113313990..113426795hg38UCSC Ensembl
Innerchr1:113856612..113969417hg19UCSC Ensembl
Innerchr1:113658135..113770940hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38112806
hg19112806
hg18112806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010110
Supporting Variants
Samples
Known GenesMAGI3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3491827
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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