A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052122



Internal ID19141341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:60626110..60651388hg38UCSC Ensembl
Innerchr13:61200244..61225522hg19UCSC Ensembl
Innerchr13:60098245..60123523hg18UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3825279
hg1925279
hg1825279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3526586, nssv3526587
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)nsv1052122
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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