A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041037



Internal ID19130256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:61716039..61763539hg38UCSC Ensembl
Innerchr13:62290172..62337672hg19UCSC Ensembl
Innerchr13:61188173..61235673hg18UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3847501
hg1947501
hg1847501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3526590
Samples
Known GenesMIR548AN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041037
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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