A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608977



Internal ID16049700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149397933..149499939hg38UCSC Ensembl
Innerchr7:149095024..149197030hg19UCSC Ensembl
Innerchr7:148725957..148827963hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38102007
hg19102007
hg18102007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11713n54
Supporting Variantsnssv1099469
Samples
Known GenesZNF746, ZNF777
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608977
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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