A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608669



Internal ID16396078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143133530..143172360hg38UCSC Ensembl
Innerchr7:142830623..142869453hg19UCSC Ensembl
Innerchr7:142540745..142579575hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3838831
hg1938831
hg1838831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11662n54
Supporting Variantsnssv1096515
Samples
Known GenesPIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608669
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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