A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610864



Internal ID16051587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:26754119..26778227hg38UCSC Ensembl
Innerchr8:26611636..26635744hg19UCSC Ensembl
Innerchr8:26667553..26691661hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3824109
hg1924109
hg1824109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1109353
Samples
Known GenesADRA1A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610864
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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