A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131074



Internal ID19285966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:100587163..100587763hg38UCSC Ensembl
Outerchr14:101053500..101054100hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1131n106
Supporting Variantsnssv3967779
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131074
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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