A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004025



Internal ID18746556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9000983..9069086hg38UCSC Ensembl
Innerchr1:9061042..9129145hg19UCSC Ensembl
Innerchr1:8983629..9051732hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3868104
hg1968104
hg1868104
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3467938
Samples
Known GenesSLC2A5, SLC2A7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004025
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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