A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953



Internal ID15550814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:131805942..131850903hg38UCSC Ensembl
Outerchr7:131490701..131535662hg19UCSC Ensembl
Outerchr7:131141241..131186202hg18UCSC Ensembl
Outerchr7:130947956..130992917hg17UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3844962
hg1944962
hg1844962
hg1744962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8429
SamplesNA12156
Known Genes
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)nsv5953
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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