A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912



Internal ID15204083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:114205615..114242472hg38UCSC Ensembl
Outerchr7:113845670..113882527hg19UCSC Ensembl
Outerchr7:113632906..113669763hg18UCSC Ensembl
Outerchr7:113439621..113476478hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3836858
hg1936858
hg1836858
hg1736858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8418
SamplesNA12156
Known GenesFOXP2
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)nsv5912
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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