A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051359



Internal ID19140578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:88606424..88659551hg38UCSC Ensembl
Innerchr13:89258679..89311805hg19UCSC Ensembl
Innerchr13:88056680..88109806hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3853128
hg1953127
hg1853127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713263
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)nsv1051359
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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