A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6650



Internal ID15204895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:104800056..104845227hg38UCSC Ensembl
Outerchr9:107562337..107607508hg19UCSC Ensembl
Outerchr9:106602158..106647329hg18UCSC Ensembl
Outerchr9:104641892..104687063hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3845172
hg1945172
hg1845172
hg1745172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8650
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)nsv6650
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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