A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047037



Internal ID19136256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:61849411..61927908hg38UCSC Ensembl
Innerchr13:62423544..62502041hg19UCSC Ensembl
Innerchr13:61321545..61400042hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3878498
hg1978498
hg1878498
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1682n100
Supporting Variantsnssv3526592
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)nsv1047037
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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