A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985805



Internal ID18879026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:20462246..20462302hg38UCSC Ensembl
Outerchr14:20930405..20930461hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127371
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985805
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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