A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121505



Internal ID19279613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:95787505..95787621hg38UCSC Ensembl
Outerchr14:96253842..96253958hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3965507
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121505
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer