A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002926



Internal ID19092143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:69196131..69239716hg38UCSC Ensembl
Innerchr4:70061849..70105434hg19UCSC Ensembl
Innerchr4:70096438..70140023hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3843586
hg1943586
hg1843586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3630290
Samples
Known GenesUGT2B11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002926
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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