A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608457



Internal ID16395866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134703503..134718989hg38UCSC Ensembl
Innerchr7:134388255..134403741hg19UCSC Ensembl
Innerchr7:134038795..134054281hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3815487
hg1915487
hg1815487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155235
SamplesHGDP00968
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608457
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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