A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4586



Internal ID15192627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:36731974..36759689hg38UCSC Ensembl
Outerchr22:37128019..37155733hg19UCSC Ensembl
Outerchr22:35457965..35485679hg18UCSC Ensembl
Outerchr22:35452519..35480233hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3827716
hg1927715
hg1827715
hg1727715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3617
Supporting Variants
SamplesNA12878
Known GenesIFT27
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)nssv4586
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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