A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986884



Internal ID19213778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:134959395..134959464hg38UCSC Ensembl
Outerchr8:135971638..135971707hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132174
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986884
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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