A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982128



Internal ID18617324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:93954416..93961076hg38UCSC Ensembl
Innerchr8:94966644..94973304hg19UCSC Ensembl
Innerchr8:95035820..95042480hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg386661
hg196661
hg186661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2761238
SamplesHGDP00778
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982128
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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