A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118293



Internal ID19254111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:102509463..102510263hg38UCSC Ensembl
Outerchr14:102975800..102976600hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980970
SamplesKWS1
Known GenesANKRD9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118293
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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