A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925



Internal ID15550783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:119164648..119201531hg38UCSC Ensembl
Outerchr7:118804702..118841585hg19UCSC Ensembl
Outerchr7:118591938..118628821hg18UCSC Ensembl
Outerchr7:118398653..118435536hg17UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3836884
hg1936884
hg1836884
hg1736884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6165
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)nsv5925
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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