A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605699



Internal ID16046422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:886312..1073232hg38UCSC Ensembl
Innerchr7:925949..1112868hg19UCSC Ensembl
Innerchr7:892475..1079394hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38186921
hg19186920
hg18186920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1077808
Samples
Known GenesADAP1, C7orf50, COX19, CYP2W1, GET4, GPR146, MIR339
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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