A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122190



Internal ID19250759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:39374281..39529681hg38UCSC Ensembl
Outerchr8:39231800..39387200hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38155401
hg19155401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3807n106
Supporting Variantsnssv3969633
SamplesKWS2
Known GenesADAM3A, ADAM5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122190
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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