A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129929



Internal ID19258053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:49491713..49491873hg38UCSC Ensembl
Outerchr14:49958431..49958591hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1080n106
Supporting Variantsnssv3965067
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129929
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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