A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049171



Internal ID19138390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105363399..105453634hg38UCSC Ensembl
Innerchr13:106015749..106105983hg19UCSC Ensembl
Innerchr13:104813750..104903984hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3890236
hg1990235
hg1890235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525561, nssv3525560
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)nsv1049171
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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