A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3792



Internal ID15201751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:44836688..44881327hg38UCSC Ensembl
Outerchr3:44878180..44922819hg19UCSC Ensembl
Outerchr3:44853184..44897823hg18UCSC Ensembl
Outerchr3:44853184..44897823hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3844640
hg1944640
hg1844640
hg1744640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7799
SamplesNA12156
Known GenesKIF15, MIR564, TGM4, TMEM42
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)nsv3792
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