A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077693



Internal ID15584193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:192302..193694hg38UCSC Ensembl
Innerchr7:192302..193694hg19UCSC Ensembl
Innerchr7:287385..288777hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381393
hg191393
hg181393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605628
Supporting Variants
Samples
Known GenesFAM20C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1077693
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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