A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113674



Internal ID18925788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:102137115..102137198hg38UCSC Ensembl
Outerchr14:102603452..102603535hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968992
SamplesKWS2
Known GenesHSP90AA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113674
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