A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980275



Internal ID18874020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:5887629..5890887hg38UCSC Ensembl
Outerchr10:5929592..5932850hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383259
hg193259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118070
Supporting Variants
SamplesKWS1
Known GenesANKRD16, FBXO18
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980275
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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