A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8638



Internal ID15535226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:97813976..97858752hg38UCSC Ensembl
Outerchr9:100576258..100621034hg19UCSC Ensembl
Outerchr9:99616079..99660855hg18UCSC Ensembl
Outerchr9:97655813..97700589hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3844777
hg1944777
hg1844777
hg1744777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6627
Supporting Variants
SamplesNA12156
Known GenesFOXE1
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)nssv8638
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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