A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3489053



Internal ID18730008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:107385172..108187137hg38UCSC Ensembl
Innerchr1:107927794..108729759hg19UCSC Ensembl
Innerchr1:107729317..108531282hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38801966
hg19801966
hg18801966
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004696
Supporting Variants
Samples
Known GenesMIR7852, NTNG1, SLC25A24, VAV3, VAV3-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3489053
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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