A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608377



Internal ID16395786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:126838136..126872460hg38UCSC Ensembl
Innerchr7:126478190..126512514hg19UCSC Ensembl
Innerchr7:126265426..126299750hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3834325
hg1934325
hg1834325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1094254
Samples
Known GenesGRM8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608377
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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