A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997692



Internal ID18846571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41624440..41624497hg38UCSC Ensembl
Outerchr15:41916638..41916695hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1148906
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997692
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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