A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7725



Internal ID15552763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:31359660..31380974hg38UCSC Ensembl
Outerchr11:31381207..31402521hg19UCSC Ensembl
Outerchr11:31337783..31359097hg18UCSC Ensembl
Outerchr11:31337783..31359097hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3821315
hg1921315
hg1821315
hg1721315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6454
SamplesNA12156
Known GenesDCDC1, DNAJC24
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)nsv7725
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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