A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001241



Internal ID19090458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:137936746..137971775hg38UCSC Ensembl
Innerchr3:137655588..137690617hg19UCSC Ensembl
Innerchr3:139138278..139173307hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3835030
hg1935030
hg1835030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4906n100
Supporting Variantsnssv3608324
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001241
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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