A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605624



Internal ID16393033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:192140..193461hg38UCSC Ensembl
Innerchr7:192140..193461hg19UCSC Ensembl
Innerchr7:287223..288544hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381322
hg191322
hg181322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11098n54
Supporting Variantsnssv1077689
Samples
Known GenesFAM20C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605624
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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