A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11207



Internal ID15539372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137316337..137334193hg38UCSC Ensembl
Outerchr9:140210789..140228645hg19UCSC Ensembl
Outerchr9:139330610..139348466hg18UCSC Ensembl
Outerchr9:137486626..137504482hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3810487
hg1910487
hg1810487
hg1710487
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6770
Supporting Variants
SamplesNA15510
Known GenesEXD3
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)nssv11207
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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