A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711769



Internal ID19010050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:61849411..61924825hg38UCSC Ensembl
Innerchr13:62423544..62498958hg19UCSC Ensembl
Innerchr13:61321545..61396959hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3875415
hg1975415
hg1875415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050841
Supporting Variants
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)nssv3711769
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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