A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6711



Internal ID15204962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:124217250..124262051hg38UCSC Ensembl
Outerchr9:126979529..127024330hg19UCSC Ensembl
Outerchr9:126019350..126064151hg18UCSC Ensembl
Outerchr9:124059083..124103884hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3844802
hg1944802
hg1844802
hg1744802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8666
SamplesNA12156
Known GenesNEK6
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)nsv6711
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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