A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121403



Internal ID18906013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:40601639..40601734hg38UCSC Ensembl
Outerchr8:40459158..40459253hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3965397
SamplesKWS2
Known GenesZMAT4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121403
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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