A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121408



Internal ID19252471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:85231788..85232571hg38UCSC Ensembl
Outerchr8:86144017..86144800hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38784
hg19784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3855n106
Supporting Variantsnssv3965401
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121408
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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