A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7756



Internal ID15189422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:44650253..44683874hg38UCSC Ensembl
Outerchr22:45046133..45079754hg19UCSC Ensembl
Outerchr22:43424797..43458418hg18UCSC Ensembl
Outerchr22:43366670..43400291hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg385817
hg195817
hg185817
hg175817
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3650
Supporting Variants
SamplesNA12156
Known GenesPRR5
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)nssv7756
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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