A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3065



Internal ID15200951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:155712977..155757733hg38UCSC Ensembl
Outerchr1:155682768..155727524hg19UCSC Ensembl
Outerchr1:153949392..153994148hg18UCSC Ensembl
Outerchr1:152495841..152540597hg17UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3844757
hg1944757
hg1844757
hg1744757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7695
SamplesNA12156
Known GenesDAP3, GON4L, MSTO2P
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)nsv3065
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