A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5034



Internal ID15542854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:154593636..154629421hg38UCSC Ensembl
Outerchr7:154385346..154421131hg19UCSC Ensembl
Outerchr7:154016279..154052064hg18UCSC Ensembl
Outerchr7:153822994..153858779hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3835786
hg1935786
hg1835786
hg1735786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015
Supporting Variants
SamplesNA19129
Known GenesDPP6
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)nssv5034
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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