A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982122



Internal ID18617318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:11378739..11390365hg38UCSC Ensembl
Innerchr8:11236248..11247874hg19UCSC Ensembl
Innerchr8:11273658..11285284hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3811627
hg1911627
hg1811627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2764666
SamplesHGDP01029
Known GenesC8orf12
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982122
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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