A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607745



Internal ID16048468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88838653..89418508hg38UCSC Ensembl
Innerchr7:88467967..89047822hg19UCSC Ensembl
Innerchr7:88305903..88885758hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38579856
hg19579856
hg18579856
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1089435
Samples
Known GenesZNF804B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607745
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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