A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4111



Internal ID15538838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:34626250..34647575hg38UCSC Ensembl
Outerchr1:35091851..35113176hg19UCSC Ensembl
Outerchr1:34864438..34885763hg18UCSC Ensembl
Outerchr1:34760944..34782269hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3821326
hg1921326
hg1821326
hg1721326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv399
Supporting Variants
SamplesNA12878
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)nssv4111
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