A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10328



Internal ID15195784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:42169202..42197574hg38UCSC Ensembl
Outerchr22:42565208..42593580hg19UCSC Ensembl
Outerchr22:40895152..40923524hg18UCSC Ensembl
Outerchr22:40889706..40918078hg17UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3811138
hg1911138
hg1811138
hg1711138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3643
Supporting Variants
SamplesNA18956
Known GenesTCF20
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)nssv10328
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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