A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6653



Internal ID15204898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:105680551..105735067hg38UCSC Ensembl
Outerchr9:108442832..108497348hg19UCSC Ensembl
Outerchr9:107482653..107537169hg18UCSC Ensembl
Outerchr9:105522387..105576903hg17UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3812562
hg1912562
hg1812562
hg1712562
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9768, nssv5174
SamplesNA18507, NA19129
Known GenesTMEM38B
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)nsv6653
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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