A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608466



Internal ID16395875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:137671905..137720035hg38UCSC Ensembl
Innerchr7:137356651..137404781hg19UCSC Ensembl
Innerchr7:137007191..137055321hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3848131
hg1948131
hg1848131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156027
Samples1780862299_A
Known GenesDGKI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608466
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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