A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7605



Internal ID15536259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:207799091..207808029hg38UCSC Ensembl
Outerchr2:208663815..208672753hg19UCSC Ensembl
Outerchr2:208372060..208380998hg18UCSC Ensembl
Outerchr2:208489321..208498259hg17UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg388939
hg198939
hg188939
hg178939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3134
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)nssv7605
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