A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041476



Internal ID19130695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:42630604..42651585hg38UCSC Ensembl
Innerchr13:43204740..43225721hg19UCSC Ensembl
Innerchr13:42102740..42123721hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3820982
hg1920982
hg1820982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1635n100
Supporting Variantsnssv3523399, nssv3523397, nssv3523398, nssv3523395, nssv3523400, nssv3523396, nssv3523394
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)nsv1041476
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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