A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3222



Internal ID15537950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:193147503..193171053hg38UCSC Ensembl
Outerchr3:192865292..192888842hg19UCSC Ensembl
Outerchr3:194347986..194371536hg18UCSC Ensembl
Outerchr3:194347994..194371544hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3823551
hg1923551
hg1823551
hg1723551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4174
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)nssv3222
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