A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612172



Internal ID16399581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:128452778..128611821hg38UCSC Ensembl
Innerchr8:129465024..129624067hg19UCSC Ensembl
Innerchr8:129534206..129693249hg18UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38159044
hg19159044
hg18159044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156877
Samples1780854206_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612172
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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