A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037954



Internal ID19127173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:60745399..60821773hg38UCSC Ensembl
Innerchr13:61319533..61395907hg19UCSC Ensembl
Innerchr13:60217534..60293908hg18UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3876375
hg1976375
hg1876375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3526588
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)nsv1037954
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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