A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655



Internal ID15550486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:21688851..21733585hg38UCSC Ensembl
Outerchr7:21728469..21773203hg19UCSC Ensembl
Outerchr7:21694994..21739728hg18UCSC Ensembl
Outerchr7:21501709..21546443hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3844735
hg1944735
hg1844735
hg1744735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8344
SamplesNA12156
Known GenesDNAH11
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)nsv5655
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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