A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046868



Internal ID19136087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:38098625..38137740hg38UCSC Ensembl
Innerchr13:38672762..38711877hg19UCSC Ensembl
Innerchr13:37570762..37609877hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3839116
hg1939116
hg1839116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523376, nssv3523377, nssv3523378
Samples
Known GenesLINC00571
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046868
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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