A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120698



Internal ID19251884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:37812552..37812663hg38UCSC Ensembl
Outerchr15:38104753..38104864hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1191n106
Supporting Variantsnssv3963131
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120698
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