A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960



Internal ID15550822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:135328399..135352480hg38UCSC Ensembl
Outerchr7:135013151..135037232hg19UCSC Ensembl
Outerchr7:134663691..134687772hg18UCSC Ensembl
Outerchr7:134470406..134494487hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3824082
hg1924082
hg1824082
hg1724082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8432
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)nsv5960
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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