A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041493



Internal ID19130712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:56452726..56537135hg38UCSC Ensembl
Innerchr13:57026860..57111269hg19UCSC Ensembl
Innerchr13:55924861..56009270hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3884410
hg1984410
hg1884410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523877
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)nsv1041493
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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