A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608915



Internal ID16396324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:145220724..145226205hg38UCSC Ensembl
Innerchr7:144917817..144923298hg19UCSC Ensembl
Innerchr7:144548750..144554231hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg385482
hg195482
hg185482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11699n54
Supporting Variantsnssv1097886, nssv1097888, nssv1097881, nssv1097879, nssv1097887, nssv1097880, nssv1097882, nssv1097889, nssv1097885, nssv1097878, nssv1097883, nssv1097884
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608915
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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