A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2153



Internal ID15546716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:78066620..78079572hg38UCSC Ensembl
Outerchr17:76062701..76075653hg19UCSC Ensembl
Outerchr17:73574296..73587248hg18UCSC Ensembl
Outerchr17:73574296..73587248hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3812953
hg1912953
hg1812953
hg1712953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7350
SamplesNA12156
Known GenesTNRC6C
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)nsv2153
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