A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605621



Internal ID16393030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:192037..193801hg38UCSC Ensembl
Innerchr7:192037..193801hg19UCSC Ensembl
Innerchr7:287120..288884hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381765
hg191765
hg181765
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11094n54
Supporting Variantsnssv1077684, nssv1077686, nssv1077685, nssv1077683
Samples
Known GenesFAM20C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605621
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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