A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607760



Internal ID16395169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89891589..89902000hg38UCSC Ensembl
Innerchr7:89520903..89531314hg19UCSC Ensembl
Innerchr7:89358839..89369250hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3810412
hg1910412
hg1810412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11495n54
Supporting Variantsnssv1089542
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607760
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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