A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006737



Internal ID18749268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136747346..136811901hg38UCSC Ensembl
Innerchr3:136466188..136530743hg19UCSC Ensembl
Innerchr3:137948878..138013433hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3864556
hg1964556
hg1864556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3607149
Samples
Known GenesSTAG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006737
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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