A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610881



Internal ID16051604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:32590824..32632792hg38UCSC Ensembl
Innerchr8:32448342..32490310hg19UCSC Ensembl
Innerchr8:32567884..32609852hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3841969
hg1941969
hg1841969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156830
Samples1780862194_A
Known GenesNRG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610881
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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