A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606338



Internal ID16393747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16670083..16743142hg38UCSC Ensembl
Innerchr7:16709708..16782767hg19UCSC Ensembl
Innerchr7:16676233..16749292hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3873060
hg1973060
hg1873060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1079627
Samples
Known GenesBZW2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606338
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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