A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022136



Internal ID19111354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:53686430..53709528hg38UCSC Ensembl
Innerchr7:53754123..53777221hg19UCSC Ensembl
Innerchr7:53721617..53744715hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3823099
hg1923099
hg1823099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661309
Samples
Known GenesFLJ45974
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022136
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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