A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564



Internal ID15551486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:73972912..74018488hg38UCSC Ensembl
Outerchr9:76587828..76633404hg19UCSC Ensembl
Outerchr9:75777648..75823224hg18UCSC Ensembl
Outerchr9:73817382..73862958hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3845577
hg1945577
hg1845577
hg1745577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6283
SamplesNA12156
Known GenesMIR6130
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)nsv6564
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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