A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605629



Internal ID16393038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:192406..193694hg38UCSC Ensembl
Innerchr7:192406..193694hg19UCSC Ensembl
Innerchr7:287489..288777hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381289
hg191289
hg181289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11098n54
Supporting Variantsnssv1077694
Samples
Known GenesFAM20C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605629
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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