A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606976



Internal ID16394385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:51527709..51549133hg38UCSC Ensembl
Innerchr7:51595406..51616830hg19UCSC Ensembl
Innerchr7:51562900..51584324hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3821425
hg1921425
hg1821425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11341n54
Supporting Variantsnssv1084565
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606976
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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