A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3609



Internal ID15548235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:175077276..175125270hg38UCSC Ensembl
Outerchr1:175046412..175094406hg19UCSC Ensembl
Outerchr1:173313035..173361029hg18UCSC Ensembl
Outerchr1:171778069..171826063hg17UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3847995
hg1947995
hg1847995
hg1747995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10357, nssv2608
SamplesNA18956, NA18555
Known GenesTNN
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)nsv3609
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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