A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608686



Internal ID16049409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143728268..143762143hg38UCSC Ensembl
Innerchr7:143425361..143459236hg19UCSC Ensembl
Innerchr7:143056294..143090169hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3833876
hg1933876
hg1833876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1096536
Samples
Known GenesCTAGE6, FAM115C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608686
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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