A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124329



Internal ID19263277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:22708859..22708909hg38UCSC Ensembl
Outerchr8:22566372..22566422hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992400, nssv3958408
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124329
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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