A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1086549



Internal ID15593049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:71774529..71801548hg38UCSC Ensembl
Innerchr7:71239514..71266533hg19UCSC Ensembl
Innerchr7:70877450..70904469hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3827020
hg1927020
hg1827020
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607459
Supporting Variants
Samples
Known GenesCALN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1086549
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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