A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625001



Internal ID15848537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:98355699..98358095hg38UCSC Ensembl
Outerchr15:98898928..98901324hg19UCSC Ensembl
Outerchr15:96716451..96718847hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382397
hg192397
hg182397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512410
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625001
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