A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7825



Internal ID15536039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:172867810..172913078hg38UCSC Ensembl
Outerchr1:172836950..172882218hg19UCSC Ensembl
Outerchr1:171103573..171148841hg18UCSC Ensembl
Outerchr1:169568607..169613875hg17UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg3845269
hg1945269
hg1845269
hg1745269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3587
Supporting Variants
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)nssv7825
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