A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1558



Internal ID15546121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:61521508..61566244hg38UCSC Ensembl
Outerchr15:61813707..61858443hg19UCSC Ensembl
Outerchr15:59600999..59645735hg18UCSC Ensembl
Outerchr15:59600999..59645735hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3844737
hg1944737
hg1844737
hg1744737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7179
SamplesNA12156
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv1558
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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