A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609123



Internal ID16396532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155264592..155288839hg38UCSC Ensembl
Innerchr7:155056302..155080549hg19UCSC Ensembl
Innerchr7:154687235..154711482hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3824248
hg1924248
hg1824248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11744n54
Supporting Variantsnssv1100263, nssv1100262, nssv1100261, nssv1100260, nssv1100264
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609123
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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