A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958747



Internal ID19207640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:17881323..17881386hg38UCSC Ensembl
Outerchr8:17738832..17738895hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128407
Supporting Variants
SamplesKWS1
Known GenesFGL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3958747
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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