A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6269



Internal ID15537594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:28453765..28499525hg38UCSC Ensembl
Outerchr9:28453763..28499523hg19UCSC Ensembl
Outerchr9:28443763..28489523hg18UCSC Ensembl
Outerchr9:28443763..28489523hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3845761
hg1945761
hg1845761
hg1745761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513
Supporting Variants
SamplesNA12156
Known GenesLINGO2
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)nssv6269
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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