A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929



Internal ID15550787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:120827537..120873418hg38UCSC Ensembl
Outerchr7:120467591..120513472hg19UCSC Ensembl
Outerchr7:120254827..120300708hg18UCSC Ensembl
Outerchr7:120061542..120107423hg17UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3845882
hg1945882
hg1845882
hg1745882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6166
SamplesNA12156
Known GenesTSPAN12
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)nsv5929
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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