A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041530



Internal ID19130749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63453454..63499844hg38UCSC Ensembl
Innerchr13:64027587..64073977hg19UCSC Ensembl
Innerchr13:62925588..62971978hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3846391
hg1946391
hg1846391
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1684n100
Supporting Variantsnssv3526606
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)nsv1041530
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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