A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6652



Internal ID15204897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:104906499..104951237hg38UCSC Ensembl
Outerchr9:107668780..107713518hg19UCSC Ensembl
Outerchr9:106708601..106753339hg18UCSC Ensembl
Outerchr9:104748335..104793073hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3844739
hg1944739
hg1844739
hg1744739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8651
SamplesNA12156
Known GenesABCA1
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)nsv6652
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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