A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9772



Internal ID15540099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:125573996..125590390hg38UCSC Ensembl
Outerchr9:128336275..128352669hg19UCSC Ensembl
Outerchr9:127376096..127392490hg18UCSC Ensembl
Outerchr9:125415829..125432223hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3820306
hg1920306
hg1820306
hg1720306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6714
Supporting Variants
SamplesNA18507
Known GenesMAPKAP1
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)nssv9772
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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