A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967137



Internal ID18895274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105180763..105181763hg38UCSC Ensembl
Outerchr14:105647100..105648100hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112655
Supporting Variants
SamplesKWS2
Known GenesNUDT14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967137
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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