A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611485



Internal ID16398894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:69905777..69945636hg38UCSC Ensembl
Innerchr8:70818012..70857871hg19UCSC Ensembl
Innerchr8:70980566..71020425hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3839860
hg1939860
hg1839860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156855
Samples1780862461_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611485
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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