A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608976



Internal ID16049699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149318278..149499939hg38UCSC Ensembl
Innerchr7:149015369..149197030hg19UCSC Ensembl
Innerchr7:148646302..148827963hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38181662
hg19181662
hg18181662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1099468
Samples
Known GenesZNF746, ZNF777
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608976
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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