A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967127



Internal ID18891842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:24398594..24399094hg38UCSC Ensembl
Outerchr14:24867800..24868300hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112645
Supporting Variants
SamplesKWS2
Known GenesNYNRIN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967127
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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