A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049556



Internal ID18792087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:46128266..46186795hg38UCSC Ensembl
Innerchr13:46702401..46760930hg19UCSC Ensembl
Innerchr13:45600402..45658931hg18UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg3858530
hg1958530
hg1858530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523428
Samples
Known GenesLCP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049556
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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