A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462



Internal ID15551374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:5699178..5743953hg38UCSC Ensembl
Outerchr9:5699178..5743953hg19UCSC Ensembl
Outerchr9:5689178..5733953hg18UCSC Ensembl
Outerchr9:5689178..5733953hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3844776
hg1944776
hg1844776
hg1744776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8580
SamplesNA12156
Known GenesKIAA1432
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)nsv6462
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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